| Total (362) | D1 (31) | D2 (85) | D3 (111) | D4 (135) | |
|---|---|---|---|---|---|
| Premier | 13 (3.59 %) | 1 (3.23 %) | 3 (3.53 %) | 1 (0.90 %) | 8 (5.93 %) |
| Deuxième | 24 (6.63 %) | 1 (3.23 %) | 7 (6.31 %) | 16 (11.85 %) | |
| Troisième | 20 (5.52 %) | 1 (1.18 %) | 5 (4.50 %) | 14 (10.37 %) |
| Eq | Saison | Div | Tour | Match | Neg | Plc | IC | ADV |
|---|---|---|---|---|---|---|---|---|
| KIH | 2014 | 4 | 10 | KIH(25.0)-PHEb(30.0) | -196 | 8 | 3.0 | 4.0 |
| KIH | 2014 | 4 | 9 | SABc(29.0)-KIH(26.0) | -215 | 5 | 6.0 | 2.0 |
| KIH | 2014 | 4 | 8 | STA(27.0)-KIH(28.0) | -130 | 8 | 3.0 | 3.0 |
| KIH | 2014 | 4 | 7 | KIH(35.0)-KAKb(20.0) | -184 | 5 | 6.0 | 1.0 |
| KIH | 2014 | 4 | 5 | PHEb(23.0)-KIH(32.0) | -116 | 4 | 7.0 | 1.0 |
| KIH | 2014 | 4 | 4 | KIH(27.0)-SABc(28.0) | -59 | 2 | 9.0 | 1.0 |
| KIH | 2014 | 4 | 3 | KIH(24.0)-STA(31.0) | -209 | 9 | 2.0 | 5.0 |
| KIH | 2014 | 4 | 2 | KAKb(16.0)-KIH(39.0) | -96 | 4 | 7.0 | 0.0 |
| KIH | 2014 | 4 | 1 | KIH(22.5)-RECa(32.5) | -214 | 4 | 6.5 | 2.5 |
| KIH | 2013 | 4 | 10 | KIH(31.0)-CINb(24.0) | -159 | 6 | 5.0 | 2.0 |
| KIH | 2013 | 4 | 9 | KIH(33.0)-QUAb(22.0) | -281 | 8 | 3.0 | 3.0 |
| KIH | 2013 | 4 | 8 | KAKb(24.0)-KIH(31.0) | -103 | 6 | 5.0 | 2.0 |
| KIH | 2013 | 4 | 7 | PHEb(25.0)-KIH(29.0) | -172 | 7 | 4.0 | 3.0 |
| KIH | 2013 | 4 | 6 | KIH(34.0)-ASS(21.0) | -131 | 4 | 7.0 | 1.0 |
| KIH | 2013 | 4 | 5 | CINb(37.0)-KIH(18.0) | -226 | 7 | 4.0 | 5.0 |
| KIH | 2013 | 4 | 4 | QUAb(31.0)-KIH(24.0) | -216 | 10 | 1.0 | 5.0 |
| KIH | 2013 | 4 | 3 | KIH(25.0)-KAKb(30.0) | -123 | 4 | 7.0 | 2.0 |
| KIH | 2013 | 4 | 2 | KIH(30.0)-PHEb(25.0) | -174 | 6 | 5.0 | 2.0 |
| KIH | 2013 | 4 | 1 | ASS(29.0)-KIH(26.0) | -211 | 6 | 5.0 | 3.0 |
| KIH | 2012 | 4 | 10 | KIH(33.0)-RECb(22.0) | -190 | 6 | 5.0 | 2.0 |
| KIH | 2012 | 4 | 9 | RECb(30.0)-KIH(25.0) | -183 | 7 | 4.0 | 4.0 |
| KIH | 2012 | 4 | 8 | KIH(31.0)-QUAa(24.0) | -218 | 9 | 2.0 | 4.0 |
| KIH | 2012 | 4 | 7 | KIH(34.0)-KAKc(21.0) | -64 | 6 | 5.0 | 2.0 |
| KIH | 2012 | 4 | 5 | QUAa(22.0)-KIH(33.0) | -120 | 3 | 8.0 | 0.0 |
| KIH | 2012 | 4 | 4 | KAKc(26.0)-KIH(29.0) | -161 | 4 | 7.0 | 1.0 |
| KIH | 2012 | 4 | 1 | RECb(23.0)-KIH(32.0) | -228 | 2 | 9.0 | 0.0 |
| KIH | 2011 | 3 | 10 | KIH(69.0)-CIN(67.0) | -171 | 14 | 2.5 | 7.5 |
| KIH | 2011 | 3 | 9 | KIH(80.0)-ASS(56.0) | -117 | 2 | 15.0 | 0.0 |
| KIH | 2011 | 3 | 8 | ACJb(92.0)-KIH(44.0) | -190 | 11 | 6.0 | 8.0 |
| KIH | 2011 | 3 | 7 | BOUa(82.0)-KIH(54.0) | -271 | 12 | 5.0 | 7.0 |
| KIH | 2011 | 3 | 6 | KIH(63.0)-HYAb(72.0) | -190 | 8 | 9.0 | 4.0 |
| KIH | 2011 | 3 | 5 | CIN(72.0)-KIH(64.0) | -143 | 9 | 8.0 | 4.0 |
| KIH | 2011 | 3 | 4 | ASS(73.5)-KIH(62.5) | -251 | 11 | 5.5 | 6.5 |
| KIH | 2011 | 3 | 3 | KIH(51.0)-ACJb(85.0) | -222 | 7 | 10.0 | 5.0 |
| KIH | 2011 | 3 | 2 | KIH(60.5)-BOUa(75.5) | -202 | 10 | 7.0 | 5.0 |
| KIH | 2011 | 3 | 1 | HYAb(78.0)-KIH(58.0) | -287 | 15 | 2.0 | 8.0 |
| KIHa | 2010 | 3 | 10 | KIHa(83.0)-SABc(28.0) | -211 | 6 | 11.0 | 2.0 |
| KIHa | 2010 | 3 | 9 | KIHa(70.5)-RECa(65.5) | -61 | 4 | 13.0 | 1.0 |
| KIHa | 2010 | 3 | 8 | CINa(71.0)-KIHa(65.0) | -226 | 13 | 4.0 | 7.0 |
| KIHa | 2010 | 3 | 7 | QUAa(55.0)-KIHa(81.0) | -173 | 10 | 7.0 | 4.0 |
| KIHa | 2010 | 3 | 6 | KIHa(68.0)-HYAb(68.0) | -103 | 5 | 12.0 | 1.0 |
| KIHa | 2010 | 3 | 5 | SABc(86.0)-KIHa(50.0) | -155 | 12 | 5.0 | 8.0 |
| KIHa | 2010 | 3 | 4 | RECa(73.0)-KIHa(63.0) | -161 | 14 | 3.0 | 7.0 |
| KIHa | 2010 | 3 | 3 | KIHa(67.0)-CINa(69.0) | -397 | 14 | 3.0 | 7.0 |
| KIHa | 2009 | 4 | 10 | YODc(21.0)-KIHa(57.0) | -186 | 7 | 0.0 | 0.0 |
| KIHa | 2009 | 4 | 9 | KIHa(57.0)-RECb(21.0) | -97 | 6 | 7.0 | 0.0 |
| KIHa | 2009 | 4 | 8 | KIHa(51.0)-SABd(27.0) | -352 | 9 | 4.0 | 3.0 |
| KIHa | 2009 | 4 | 7 | SABd(25.0)-KIHa(53.0) | -244 | 5 | 8.0 | 1.0 |
| KIHa | 2009 | 4 | 5 | KIHa(49.5)-YODc(28.5) | -107 | 3 | 10.0 | 1.0 |
| KIHa | 2009 | 4 | 4 | KIHa(42.0)-RECb(36.0) | -151 | 10 | 3.0 | 5.0 |
| KIHa | 2009 | 4 | 3 | YODc(22.0)-KIHa(56.0) | -189 | 3 | 9.5 | 0.0 |
| KIHa | 2009 | 4 | 2 | KIHa(50.0)-SABd(28.0) | -181 | 5 | 8.0 | 1.0 |
| KIHa | 2009 | 4 | 1 | RECb(23.0)-KIHa(55.0) | -88 | 2 | 11.0 | 0.0 |
| KIHa | 2008 | 3 | 10 | KIHa(62.0)-RECa(74.0) | -144 | 11 | 6.0 | 6.0 |
| KIHa | 2008 | 3 | 9 | HYAb(71.0)-KIHa(65.0) | -156 | 15 | 2.0 | 7.0 |
| KIHa | 2008 | 3 | 8 | KIHa(57.0)-SABc(79.0) | -134 | 8 | 9.0 | 5.0 |
| KIHa | 2008 | 3 | 7 | ACJb(56.0)-KIHa(80.0) | -122 | 9 | 8.0 | 3.0 |
| KIHa | 2008 | 3 | 6 | KIHa(50.0)-KAKa(86.0) | -99 | 7 | 10.0 | 5.0 |
| KIHa | 2008 | 3 | 5 | RECa(71.0)-KIHa(65.0) | -228 | 11 | 6.0 | 7.0 |
| KIHa | 2008 | 3 | 4 | KIHa(74.0)-HYAb(61.0) | -81 | 9 | 8.0 | 5.0 |
| KIHa | 2008 | 3 | 3 | SABc(61.0)-KIHa(74.0) | -161 | 11 | 6.0 | 5.0 |
| KIHa | 2008 | 3 | 2 | KIHa(62.0)-ACJb(74.0) | -224 | 16 | 1.0 | 8.0 |
| KIHa | 2008 | 3 | 1 | KAKa(77.0)-KIHa(59.0) | -95 | 6 | 11.0 | 4.0 |
| KIHa | 2007 | 4 | 10 | NUPa(43.5)-KIHa(34.5) | -109 | 3 | 10.0 | 1.0 |
| KIHa | 2007 | 4 | 9 | KIHa(54.0)-PHEb(24.0) | -140 | 5 | 8.0 | 1.0 |
| KIHa | 2007 | 4 | 8 | KIHa(48.0)-CINa(30.0) | -152 | 5 | 8.0 | 2.0 |
| KIHa | 2007 | 4 | 7 | ACJc(36.0)-KIHa(42.0) | -355 | 16 | 0.0 | 8.0 |
| KIHa | 2007 | 4 | 6 | KIHa(56.0)-KIHb(22.0) | -204 | 13 | 0.0 | 5.0 |
| KIHa | 2007 | 4 | 5 | KIHa(40.0)-NUPa(38.0) | -234 | 7 | 6.0 | 3.0 |
| KIHa | 2007 | 4 | 4 | PHEb(23.0)-KIHa(55.0) | -124 | 3 | 10.0 | 0.0 |
| KIHa | 2007 | 4 | 2 | KIHa(55.0)-ACJc(23.0) | -94 | 4 | 9.0 | 0.0 |
| KIHa | 2007 | 4 | 1 | KIHb(21.0)-KIHa(57.0) | -278 | 6 | 7.0 | 0.0 |
| KIHa | 2006 | 4 | 10 | KIHa(39.0)-ACJb(39.0) | -168 | 12 | 1.0 | 6.0 |
| KIHa | 2006 | 4 | 9 | MAKb(25.0)-KIHa(53.0) | -220 | 15 | 0.0 | 7.0 |
| KIHa | 2006 | 4 | 8 | GELa(51.0)-KIHa(27.0) | -297 | 10 | 3.0 | 6.0 |
| KIHa | 2006 | 4 | 7 | KIHa(57.0)-LAPb(21.0) | -105 | 4 | 9.0 | 0.0 |
| KIHa | 2006 | 4 | 6 | DJIa(24.0)-KIHa(54.0) | -162 | 2 | 11.0 | 0.0 |
| KIHa | 2006 | 4 | 5 | ACJb(39.0)-KIHa(39.0) | -99 | 6 | 7.0 | 3.0 |
| KIHa | 2006 | 4 | 4 | KIHa(48.0)-MAKb(30.0) | -318 | 7 | 6.0 | 2.0 |
| KIHa | 2006 | 4 | 3 | KIHa(44.0)-GELa(34.0) | -154 | 5 | 8.0 | 2.0 |
| KIHa | 2006 | 4 | 2 | LAPb(21.0)-KIHa(57.0) | -128 | 3 | 9.5 | 0.0 |
| KIHa | 2006 | 4 | 1 | KIHa(52.0)-DJIa(26.0) | -248 | 7 | 6.0 | 2.0 |
| KIHa | 2005 | 3 | 10 | HELa(87.0)-KIHa(49.0) | -154 | 6 | 11.0 | 4.0 |
| KIHa | 2005 | 3 | 9 | KIHa(42.5)-CHIb(93.5) | -256 | 16 | 1.0 | 8.0 |
| KIHa | 2005 | 3 | 8 | KIHa(49.5)-ROYb(86.5) | -160 | 13 | 4.0 | 7.0 |
| KIHa | 2005 | 3 | 7 | PHEa(81.0)-KIHa(55.0) | -211 | 6 | 11.0 | 4.0 |
| KIHa | 2005 | 3 | 6 | KIHa(76.0)-MAKa(59.0) | -95 | 7 | 10.0 | 2.0 |
| KIHa | 2005 | 3 | 5 | KIHa(47.0)-HELa(89.0) | -249 | 12 | 4.5 | 8.0 |
| KIHa | 2005 | 3 | 4 | CHIb(76.0)-KIHa(60.0) | -173 | 15 | 2.0 | 8.0 |
| KIHa | 2005 | 3 | 3 | ROYb(90.0)-KIHa(46.0) | -226 | 12 | 5.0 | 8.0 |
| KIHa | 2005 | 3 | 2 | KIHa(65.5)-PHEa(70.5) | -153 | 8 | 9.0 | 4.0 |
| KIHa | 2005 | 3 | 1 | MAKa(74.0)-KIHa(62.0) | -58 | 2 | 15.0 | 0.0 |
| KIHa | 2004 | 3 | 10 | ESCa(62.0)-KIHa(73.0) | -178 | 7 | 10.0 | 3.0 |
| KIHa | 2004 | 3 | 9 | KIHa(67.0)-CHIb(69.0) | -96 | 5 | 11.5 | 3.0 |
| KIHa | 2004 | 3 | 8 | KIHa(70.0)-REJa(66.0) | -225 | 10 | 7.0 | 5.0 |
| KIHa | 2004 | 3 | 7 | KIHa(58.0)-ROYb(78.0) | -245 | 11 | 6.0 | 5.0 |
| KIHa | 2004 | 3 | 6 | VRAa(63.0)-KIHa(73.0) | -195 | 5 | 12.0 | 2.0 |
| KIHa | 2004 | 3 | 5 | KIHa(73.5)-ESCa(62.5) | -100 | 8 | 9.0 | 3.0 |
| KIHa | 2004 | 3 | 4 | CHIb(62.0)-KIHa(74.0) | -71 | 4 | 12.5 | 1.0 |
| KIHa | 2004 | 3 | 3 | REJa(74.0)-KIHa(62.0) | -41 | 4 | 13.0 | 2.0 |
| KIHa | 2004 | 3 | 2 | ROYb(72.0)-KIHa(64.0) | -286 | 10 | 7.0 | 5.0 |
| KIHa | 2004 | 3 | 1 | KIHa(67.0)-VRAa(69.0) | -120 | 1 | 16.0 | 0.0 |
| KIHa | 2003 | 3 | 10 | KIHa(68.0)-JOKa(65.0) | -153 | 9 | 8.0 | 4.0 |
| KIHa | 2003 | 3 | 9 | ESCa(68.0)-KIHa(68.0) | -150 | 4 | 13.0 | 1.0 |
| KIHa | 2003 | 3 | 8 | LOUa(45.0)-KIHa(91.0) | -123 | 7 | 10.0 | 1.0 |
| KIHa | 2003 | 3 | 7 | KIHa(55.0)-JAQa(81.0) | -246 | 14 | 3.0 | 8.0 |
| KIHa | 2003 | 3 | 5 | JOKa(61.5)-KIHa(74.5) | -55 | 6 | 11.0 | 2.0 |
| KIHa | 2003 | 3 | 4 | KIHa(78.0)-ESCa(58.0) | -115 | 9 | 8.0 | 4.0 |
| KIHa | 2003 | 3 | 3 | KIHa(74.5)-LOUa(61.5) | -56 | 5 | 12.0 | 2.0 |
| KIHa | 2003 | 3 | 2 | JAQa(48.0)-KIHa(88.0) | -82 | 3 | 14.0 | 0.0 |
| KIHa | 2002 | 3 | 10 | CRSa(72.0)-KIHa(64.0) | -78 | 2 | 15.0 | 1.0 |
| KIHa | 2002 | 3 | 9 | KIHa(61.0)-ASSa(74.0) | -108 | 3 | 14.0 | 2.0 |
| KIHa | 2002 | 3 | 8 | CHIb(75.0)-KIHa(61.0) | -190 | 16 | 1.0 | 8.0 |
| KIHa | 2002 | 3 | 7 | KIHa(58.5)-BLOa(77.5) | -241 | 9 | 7.5 | 5.0 |
| KIHa | 2002 | 3 | 6 | QUAa(69.0)-KIHa(67.0) | -146 | 13 | 4.0 | 6.0 |
| KIHa | 2002 | 3 | 5 | KIHa(63.0)-CRSa(72.0) | -226 | 11 | 6.0 | 6.0 |
| KIHa | 2002 | 3 | 4 | ASSa(57.0)-KIHa(78.0) | -121 | 5 | 12.0 | 1.0 |
| KIHa | 2002 | 3 | 3 | KIHa(77.0)-CHIb(58.0) | -136 | 11 | 6.0 | 5.0 |
| KIHa | 2002 | 3 | 2 | BLOa(64.0)-KIHa(71.0) | -432 | 14 | 3.0 | 7.0 |
| KIHa | 2002 | 3 | 1 | KIHa(64.0)-QUAa(72.0) | -132 | 11 | 6.0 | 6.0 |
| KIHa | 2001 | 2 | 11 | ROYa(71.0)-KIHa(65.0) | -183 | 16 | 1.0 | 8.0 |
| KIHa | 2001 | 2 | 10 | KIHa(53.5)-SABb(82.5) | -304 | 16 | 1.0 | 8.0 |
| KIHa | 2001 | 2 | 9 | KIHa(55.0)-BRAb(81.0) | -73 | 8 | 9.0 | 5.0 |
| KIHa | 2001 | 2 | 8 | KIHa(62.0)-CHIb(74.0) | -306 | 16 | 1.0 | 8.0 |
| KIHa | 2001 | 2 | 7 | KIHa(61.0)-YODb(75.0) | -133 | 12 | 5.0 | 6.0 |
| KIHa | 2001 | 2 | 6 | KIHa(69.0)-ASSa(67.0) | -51 | 5 | 12.0 | 2.0 |
| KIHa | 2001 | 2 | 5 | BIZa(81.0)-KIHa(55.0) | -93 | 7 | 10.0 | 5.0 |
| KIHa | 2001 | 2 | 4 | KIHa(79.5)-GIBa(56.5) | -74 | 9 | 8.0 | 4.0 |
| KIHa | 2001 | 2 | 3 | JAQa(80.0)-KIHa(56.0) | -111 | 15 | 2.0 | 8.0 |
| KIHa | 2001 | 2 | 2 | HYAa(75.0)-KIHa(61.0) | -328 | 16 | 1.0 | 8.0 |
| KIHb | 2001 | 4 | 1 | KIHb(30.0)-FUNa(48.0) | -254 | 7 | 6.0 | 4.0 |
| KIHa | 2000 | 2 | 11 | SONa(81.0)-KIHa(55.0) | -193 | 13 | 4.0 | 8.0 |
| KIHa | 2000 | 2 | 10 | GIBa(69.0)-KIHa(67.0) | -167 | 13 | 4.0 | 7.0 |
| KIHa | 2000 | 2 | 9 | KIHa(54.5)-BIZa(81.5) | -268 | 15 | 2.0 | 8.0 |
| KIHa | 2000 | 2 | 8 | KIHa(64.0)-WATb(72.0) | -175 | 12 | 5.0 | 6.0 |
| KIHa | 2000 | 2 | 7 | KIHa(81.0)-PHEa(55.0) | -135 | 6 | 11.0 | 2.0 |
| KIHa | 2000 | 2 | 6 | SABb(76.5)-KIHa(59.5) | -157 | 10 | 6.5 | 6.5 |
| KIHa | 2000 | 2 | 5 | YODb(57.0)-KIHa(79.0) | -165 | 13 | 4.0 | 5.0 |
| KIHa | 2000 | 2 | 4 | BRAb(73.0)-KIHa(63.0) | -284 | 16 | 1.0 | 8.0 |
| KIHa | 2000 | 2 | 3 | KIHa(74.0)-JAQa(62.0) | -227 | 15 | 2.0 | 7.0 |
| KIHa | 2000 | 2 | 2 | KIHa(71.0)-ACJa(65.0) | -177 | 14 | 3.0 | 6.0 |
| KIHa | 2000 | 2 | 1 | MJAa(76.0)-KIHa(60.0) | -172 | 14 | 3.0 | 8.0 |
| KIHa | 1999 | 2 | 11 | ASSa(60.0)-KIHa(76.0) | -155 | 8 | 9.0 | 3.0 |
| KIHa | 1999 | 2 | 10 | KIHa(70.0)-LOUa(66.0) | -145 | 10 | 7.0 | 5.0 |
| KIHa | 1999 | 2 | 9 | KIHa(63.5)-MOUb(72.5) | -92 | 8 | 9.0 | 4.0 |
| KIHa | 1999 | 2 | 8 | HYAa(70.5)-KIHa(65.5) | -156 | 16 | 1.0 | 8.0 |
| KIHa | 1999 | 2 | 7 | KIHa(64.0)-YODb(72.0) | -143 | 14 | 3.0 | 7.0 |
| KIHa | 1999 | 2 | 6 | MATa(65.0)-KIHa(71.0) | -105 | 15 | 2.0 | 7.0 |
| KIHa | 1999 | 2 | 5 | KIHa(49.5)-SONa(86.5) | -121 | 14 | 3.0 | 8.0 |
| KIHa | 1999 | 2 | 4 | JAQa(68.5)-KIHa(67.5) | -65 | 12 | 5.0 | 5.0 |
| KIHa | 1999 | 2 | 3 | KIHa(71.5)-GIBa(64.5) | -160 | 15 | 2.0 | 8.0 |
| KIHa | 1999 | 2 | 2 | KIHa(69.0)-SABb(67.0) | -245 | 14 | 3.0 | 7.0 |
| KIHa | 1999 | 2 | 1 | KIHa(64.0)-MJAa(72.0) | -169 | 10 | 7.0 | 5.0 |
| KIHb | 1998 | 4 | 10 | KIHb(39.0)-HYAb(39.0) | -214 | 3 | 10.0 | 2.0 |
| KIHb | 1998 | 4 | 9 | SABd(28.0)-KIHb(50.0) | -229 | 2 | 11.0 | 0.0 |
| KIHc | 1998 | 4 | 8 | PHEb(48.0)-KIHc(30.0) | -106 | 1 | 12.0 | 0.0 |
| KIHb | 1998 | 4 | 7 | RECb(32.0)-KIHb(45.0) | -170 | 5 | 8.0 | 2.0 |
| KIHb | 1998 | 4 | 6 | KIHb(51.0)-QUAb(27.0) | -81 | 2 | 11.0 | 0.0 |
| KIHb | 1998 | 4 | 5 | HYAb(44.0)-KIHb(34.0) | -127 | 7 | 6.0 | 4.0 |
| KIHb | 1998 | 4 | 4 | KIHb(45.0)-SABd(33.0) | -209 | 7 | 6.0 | 2.0 |
| KIHc | 1998 | 4 | 3 | KIHc(27.0)-PHEb(51.0) | -248 | 5 | 8.0 | 3.0 |
| KIHb | 1998 | 4 | 2 | KIHb(46.0)-RECb(32.0) | -153 | 1 | 12.0 | 0.0 |
| KIHb | 1998 | 4 | 1 | QUAb(33.5)-KIHb(44.5) | -286 | 9 | 4.0 | 3.0 |
| KIHb | 1997 | 4 | 10 | YODd(23.0)-KIHb(55.0) | -95 | 2 | 11.0 | 0.0 |
| KIHb | 1997 | 4 | 9 | KIHb(27.0)-PHEa(51.0) | -241 | 11 | 3.0 | 7.0 |
| KIHb | 1997 | 4 | 8 | KAKa(41.0)-KIHb(37.0) | -162 | 5 | 8.0 | 2.0 |
| KIHa | 1997 | 2 | 7 | KIHa(62.0)-ACJa(74.0) | -183 | 14 | 3.0 | 7.0 |
| KIHb | 1997 | 4 | 5 | KIHb(53.0)-YODd(26.0) | -105 | 1 | 16.0 | 0.0 |
| KIHb | 1997 | 4 | 4 | PHEa(56.0)-KIHb(22.0) | -175 | 10 | 5.0 | 8.0 |
| KIHb | 1997 | 4 | 3 | KIHb(47.5)-KAKa(30.5) | -37 | 1 | 12.0 | 0.0 |
| KIHb | 1997 | 4 | 2 | SABd(29.0)-KIHb(49.0) | -158 | 8 | 5.0 | 2.0 |
| KIHb | 1996 | 4 | 9 | KIHb(84.0)-SASb(52.0) | -87 | 1 | 16.0 | 0.0 |
| KIHb | 1996 | 4 | 8 | SRMa(82.0)-KIHb(54.0) | -70 | 6 | 11.0 | 4.0 |
| KIHb | 1996 | 4 | 7 | KIHb(82.0)-AMAb(51.0) | -30 | 1 | 16.0 | 0.0 |
| KIHb | 1996 | 4 | 5 | KIHb(53.0)-ASSb(83.0) | -97 | 2 | 15.0 | 1.0 |
| KIHb | 1996 | 4 | 4 | SASb(51.0)-KIHb(85.0) | Top | 1 | 16.0 | 0.0 |
| KIHb | 1996 | 4 | 3 | KIHb(73.0)-SRMa(63.0) | -213 | 10 | 7.0 | 4.0 |
| KIHb | 1996 | 4 | 2 | AMAb(58.0)-KIHb(77.0) | -148 | 5 | 12.0 | 1.0 |
| KIHb | 1995 | 4 | 9 | KIHb(62.0)-SABc(74.0) | -132 | 3 | 14.0 | 2.0 |
| KIHb | 1995 | 4 | 8 | KIHb(74.0)-ASSb(61.0) | -105 | 5 | 12.0 | 2.0 |
| KIHa | 1995 | 2 | 7 | KIHa(84.0)-FUNa(52.0) | -83 | 9 | 7.5 | 3.0 |
| KIHb | 1995 | 4 | 6 | KIHb(56.0)-AMAa(80.0) | -27 | 1 | 16.0 | 0.0 |
| KIHb | 1995 | 4 | 5 | KIHb(92.0)-FUNb(44.0) | -200 | 3 | 14.0 | 0.0 |
| KIHb | 1995 | 4 | 4 | SABc(60.0)-KIHb(76.0) | -59 | 2 | 15.0 | 0.0 |
| KIHb | 1995 | 4 | 3 | ASSb(80.0)-KIHb(56.0) | -121 | 4 | 13.0 | 2.0 |
| KIHb | 1995 | 4 | 1 | AMAa(69.5)-KIHb(66.5) | -163 | 10 | 6.5 | 4.5 |
| KIHa | 1994 | 2 | 11 | SONa(75.0)-KIHa(61.0) | -98 | 16 | 1.0 | 8.0 |
| KIHa | 1994 | 2 | 10 | KIHa(68.5)-MACa(67.5) | -161 | 13 | 4.0 | 6.0 |
| KIHa | 1994 | 2 | 9 | KIHa(72.0)-MATa(64.0) | -149 | 16 | 1.0 | 8.0 |
| KIHa | 1994 | 2 | 8 | SABb(49.5)-KIHa(86.5) | -134 | 15 | 2.0 | 7.0 |
| KIHa | 1994 | 2 | 7 | ACJa(71.5)-KIHa(64.5) | -290 | 15 | 2.0 | 7.0 |
| KIHb | 1994 | 4 | 6 | KIHb(58.0)-CINa(78.0) | -187 | 8 | 9.0 | 5.0 |
| KIHa | 1994 | 2 | 5 | KIHa(67.0)-LOUa(69.0) | -161 | 13 | 4.0 | 7.0 |
| KIHa | 1994 | 2 | 4 | KIHa(54.0)-CHIa(82.0) | -146 | 8 | 9.0 | 5.0 |
| KIHa | 1994 | 2 | 3 | WATb(63.0)-KIHa(73.0) | -146 | 15 | 2.0 | 7.0 |
| KIHa | 1994 | 2 | 2 | JAQa(46.0)-KIHa(90.0) | -65 | 8 | 9.0 | 2.0 |
| KIHa | 1994 | 2 | 1 | KIHa(61.0)-PICa(75.0) | -209 | 16 | 1.0 | 8.0 |
| KIHb | 1993 | 4 | 10 | KIHb(53.0)-KAKa(83.0) | -181 | 6 | 11.0 | 4.0 |
| KIHb | 1993 | 4 | 9 | ASSb(70.0)-KIHb(66.0) | -203 | 9 | 8.0 | 4.0 |
| KIHb | 1993 | 4 | 7 | AMAb(49.0)-KIHb(87.0) | -132 | 4 | 13.0 | 0.0 |
| KIHb | 1993 | 4 | 6 | KAKa(59.5)-KIHb(76.5) | -96 | 2 | 15.0 | 0.0 |
| KIHb | 1993 | 4 | 5 | KIHb(52.5)-ASSb(83.5) | -100 | 8 | 9.0 | 5.0 |
| KIHb | 1993 | 4 | 3 | KIHb(64.0)-KAKa(72.0) | -207 | 9 | 7.5 | 5.5 |
| KIHb | 1993 | 4 | 2 | ASSb(85.0)-KIHb(51.0) | -85 | 2 | 15.0 | 1.0 |
| KIHb | 1993 | 4 | 1 | AMAb(60.0)-KIHb(76.0) | -180 | 9 | 8.0 | 4.0 |
| KIHa | 1992 | 2 | 11 | KIHa(75.0)-ASSa(61.0) | -147 | 12 | 5.0 | 5.0 |
| KIHb | 1992 | 4 | 10 | KIHb(76.0)-AMAb(60.0) | -131 | 2 | 15.0 | 0.0 |
| KIHb | 1992 | 4 | 9 | ANGa(66.0)-KIHb(70.0) | -57 | 2 | 15.0 | 1.0 |
| KIHb | 1992 | 4 | 8 | KIHb(81.0)-CHEb(55.0) | -237 | 6 | 11.0 | 2.0 |
| KIHb | 1992 | 4 | 7 | AMAa(66.5)-KIHb(69.5) | -219 | 8 | 9.0 | 3.0 |
| KIHb | 1992 | 4 | 6 | KIHb(58.5)-KAKa(77.5) | -265 | 13 | 4.0 | 6.0 |
| KIHb | 1992 | 4 | 5 | AMAb(53.0)-KIHb(83.0) | -134 | 6 | 11.0 | 1.0 |
| KIHb | 1992 | 4 | 4 | KIHb(79.5)-ANGa(56.5) | -80 | 4 | 13.0 | 1.0 |
| KIHb | 1992 | 4 | 3 | CHEb(62.0)-KIHb(74.0) | -133 | 7 | 10.0 | 3.0 |
| KIHb | 1992 | 4 | 2 | KIHb(58.0)-AMAa(78.0) | -284 | 12 | 5.0 | 6.0 |
| KIHa | 1992 | 2 | 1 | SONa(63.0)-KIHa(73.0) | -444 | 16 | 1.0 | 8.0 |
| KIHb | 1991 | 3 | 10 | MJAa(68.0)-KIHb(68.0) | -62 | 6 | 11.0 | 3.0 |
| KIHb | 1991 | 3 | 9 | KIHb(81.0)-SASa(55.0) | -108 | 6 | 11.0 | 2.0 |
| KIHb | 1991 | 3 | 8 | SIRc(73.0)-KIHb(63.0) | -15 | 2 | 15.0 | 1.0 |
| KIHb | 1991 | 3 | 7 | KIHb(53.0)-SIRb(83.0) | -119 | 13 | 4.0 | 7.0 |
| KIHb | 1991 | 3 | 6 | PHOa(76.0)-KIHb(60.0) | -110 | 5 | 12.0 | 4.0 |
| KIHb | 1991 | 3 | 5 | KIHb(81.0)-MJAa(55.0) | -51 | 4 | 12.5 | 0.0 |
| KIHb | 1991 | 3 | 4 | SASa(91.0)-KIHb(45.0) | -91 | 8 | 9.0 | 5.0 |
| KIHb | 1991 | 3 | 3 | KIHb(66.0)-SIRc(70.0) | -144 | 9 | 8.0 | 5.0 |
| KIHb | 1991 | 3 | 2 | SIRb(83.5)-KIHb(52.5) | -101 | 5 | 12.0 | 3.0 |
| KIHb | 1991 | 3 | 1 | KIHb(80.0)-PHOa(56.0) | -157 | 7 | 10.0 | 1.0 |
| KIHb | 1990 | 2 | 11 | KIHb(68.5)-SABb(67.5) | -196 | 12 | 5.0 | 6.0 |
| KIHb | 1990 | 2 | 10 | LECa(79.0)-KIHb(57.0) | -74 | 8 | 9.0 | 5.0 |
| KIHb | 1990 | 2 | 9 | CHIa(76.5)-KIHb(59.5) | -217 | 6 | 11.0 | 4.0 |
| KIHb | 1990 | 2 | 8 | KIHb(44.0)-MOUa(92.0) | -181 | 14 | 3.0 | 8.0 |
| KIHb | 1990 | 2 | 7 | SONa(86.5)-KIHb(49.5) | -196 | 15 | 2.0 | 8.0 |
| KIHb | 1990 | 2 | 6 | ACJa(89.0)-KIHb(47.0) | -166 | 13 | 4.0 | 8.0 |
| KIHb | 1990 | 2 | 5 | KIHb(56.0)-NDPa(80.0) | -103 | 6 | 11.0 | 4.0 |
| KIHb | 1990 | 2 | 4 | ASSa(79.0)-KIHb(57.0) | -288 | 12 | 5.0 | 7.0 |
| KIHb | 1990 | 2 | 3 | KIHb(55.5)-JAQa(80.5) | -165 | 8 | 9.0 | 4.0 |
| KIHb | 1990 | 2 | 2 | OUEb(66.0)-KIHb(70.0) | -265 | 16 | 1.0 | 8.0 |
| KIHb | 1990 | 2 | 1 | KIHb(46.0)-KIHa(90.0) | -117 | 13 | 4.0 | 8.0 |
| KIHb | 1989 | 3 | 10 | BLOa(68.5)-KIHb(67.5) | -209 | 12 | 5.0 | 5.0 |
| KIHb | 1989 | 3 | 9 | KIHb(93.5)-CHEa(42.5) | -185 | 7 | 10.0 | 1.0 |
| KIHb | 1989 | 3 | 8 | HYAb(74.0)-KIHb(62.0) | -198 | 14 | 3.0 | 7.0 |
| KIHb | 1989 | 3 | 7 | KIHb(89.0)-HELb(47.0) | -284 | 15 | 2.0 | 7.0 |
| KIHb | 1989 | 3 | 6 | ASSb(59.0)-KIHb(77.0) | -152 | 4 | 13.0 | 1.0 |
| KIHb | 1989 | 3 | 5 | KIHb(67.0)-BLOa(69.0) | -254 | 14 | 3.0 | 6.0 |
| KIHb | 1989 | 3 | 4 | CHEa(65.0)-KIHb(71.0) | -98 | 6 | 11.0 | 3.0 |
| KIHb | 1989 | 3 | 3 | KIHb(69.0)-HYAb(67.0) | -91 | 13 | 4.0 | 6.0 |
| KIHb | 1989 | 3 | 2 | HELb(62.0)-KIHb(74.0) | -94 | 3 | 14.0 | 1.0 |
| KIHb | 1989 | 3 | 1 | KIHb(69.0)-ASSb(67.0) | -104 | 6 | 11.0 | 2.0 |
| KIHb | 1988 | 3 | 10 | KIHb(79.0)-SASa(57.0) | -94 | 4 | 13.0 | 1.0 |
| KIHb | 1988 | 3 | 9 | YODa(85.0)-KIHb(51.0) | -185 | 15 | 2.0 | 8.0 |
| KIHb | 1988 | 3 | 8 | KIHb(63.0)-ASSb(73.0) | -223 | 12 | 4.5 | 6.0 |
| KIHb | 1988 | 3 | 7 | BLOa(52.0)-KIHb(84.0) | -98 | 5 | 12.0 | 1.0 |
| KIHb | 1988 | 3 | 6 | KIHb(81.0)-CHEa(55.0) | -201 | 9 | 8.0 | 3.0 |
| KIHb | 1988 | 3 | 5 | SASa(49.0)-KIHb(87.0) | -92 | 3 | 14.0 | 0.0 |
| KIHb | 1988 | 3 | 4 | KIHb(73.0)-YODa(63.0) | -20 | 2 | 15.0 | 1.0 |
| KIHb | 1988 | 3 | 3 | ASSb(86.0)-KIHb(50.0) | -158 | 16 | 1.0 | 8.0 |
| KIHb | 1988 | 3 | 2 | KIHb(77.5)-BLOa(57.5) | -89 | 6 | 11.0 | 2.0 |
| KIHb | 1988 | 3 | 1 | CHEa(74.0)-KIHb(62.0) | -238 | 13 | 4.0 | 6.0 |
| KIHb | 1987 | 3 | 10 | KIHb(79.0)-CSHa(57.0) | -116 | 6 | 11.0 | 2.0 |
| KIHb | 1987 | 3 | 9 | SASa(84.0)-KIHb(52.0) | -119 | 10 | 7.0 | 6.0 |
| KIHb | 1987 | 3 | 8 | KIHb(50.0)-ACJa(86.0) | -202 | 13 | 4.0 | 7.0 |
| KIHb | 1987 | 3 | 7 | BLOa(58.5)-KIHb(77.5) | -39 | 2 | 15.0 | 1.0 |
| KIHb | 1987 | 3 | 6 | KIHb(54.0)-YODa(82.0) | -66 | 9 | 8.0 | 5.0 |
| KIHb | 1987 | 3 | 5 | CSHa(53.0)-KIHb(83.0) | -88 | 2 | 15.0 | 0.0 |
| KIHb | 1987 | 3 | 4 | KIHb(59.0)-SASa(77.0) | -230 | 15 | 2.0 | 8.0 |
| KIHb | 1987 | 3 | 3 | ACJa(97.0)-KIHb(39.0) | -111 | 7 | 10.0 | 6.0 |
| KIHb | 1987 | 3 | 2 | KIHb(67.0)-BLOa(69.0) | -40 | 3 | 14.0 | 2.0 |
| KIHb | 1987 | 3 | 1 | YODa(81.0)-KIHb(55.0) | -198 | 10 | 7.0 | 6.0 |
| KIHb | 1986 | 4 | 9 | KIHb(96.0)-ANGa(40.0) | -101 | 6 | 10.5 | 1.0 |
| KIHb | 1986 | 4 | 8 | KAKa(38.0)-KIHb(98.0) | -112 | 5 | 12.0 | 0.0 |
| KIHb | 1986 | 4 | 7 | ASSc(74.5)-KIHb(61.5) | -101 | 5 | 12.0 | 3.0 |
| KIHb | 1986 | 4 | 6 | KIHb(91.0)-ANGa(45.0) | -56 | 2 | 15.0 | 0.0 |
| KIHb | 1986 | 4 | 5 | KIHb(88.0)-KAKa(48.0) | -137 | 4 | 13.0 | 1.0 |
| KIHb | 1986 | 4 | 4 | ASSc(61.0)-KIHb(75.0) | -130 | 3 | 14.0 | 1.0 |
| KIHb | 1986 | 4 | 3 | ANGa(56.0)-KIHb(80.0) | -154 | 5 | 12.0 | 2.0 |
| KIHb | 1986 | 4 | 2 | KIHb(92.0)-KAKa(44.0) | -126 | 2 | 15.0 | 0.0 |
| KIHb | 1986 | 4 | 1 | KIHb(81.5)-ASSc(54.5) | -127 | 3 | 13.5 | 0.0 |
| KIHb | 1985 | 4 | 10 | CINa(69.5)-KIHb(66.5) | -171 | 4 | 13.0 | 2.0 |
| KIHb | 1985 | 4 | 9 | KIHb(83.0)-SRMa(53.0) | -217 | 5 | 12.0 | 1.0 |
| KIHb | 1985 | 4 | 8 | ACJb(59.5)-KIHb(76.5) | -140 | 7 | 10.0 | 3.0 |
| KIHb | 1985 | 4 | 7 | KIHb(80.5)-HELb(55.5) | -44 | 5 | 12.0 | 1.0 |
| KIHb | 1985 | 4 | 6 | SASa(70.0)-KIHb(66.0) | -107 | 8 | 9.0 | 4.0 |
| KIHb | 1985 | 4 | 5 | KIHb(73.0)-CINa(63.0) | -122 | 2 | 15.0 | 1.0 |
| KIHb | 1985 | 4 | 4 | SRMa(60.0)-KIHb(76.0) | -127 | 4 | 12.5 | 2.0 |
| KIHb | 1985 | 4 | 3 | KIHb(77.0)-ACJb(59.0) | -152 | 14 | 3.0 | 7.0 |
| KIHb | 1985 | 4 | 2 | HELb(62.0)-KIHb(74.0) | -197 | 15 | 2.0 | 7.0 |
| KIHb | 1985 | 4 | 1 | KIHb(66.0)-SASa(70.0) | -136 | 8 | 9.0 | 4.0 |
| KIHb | 1984 | 4 | 14 | ACJb(38.5)-KIHb(97.5) | -71 | 3 | 14.0 | 0.0 |
| KIHb | 1984 | 4 | 13 | KIHb(91.0)-CINa(45.0) | -139 | 7 | 10.0 | 1.0 |
| KIHb | 1984 | 4 | 12 | KIHb(83.0)-ACJb(53.0) | -190 | 6 | 10.5 | 2.0 |
| KIHb | 1984 | 4 | 11 | KIHc(44.0)-KIHb(92.0) | -115 | 3 | 14.0 | 0.0 |
| KIHb | 1984 | 4 | 10 | KIHb(97.0)-SRMa(39.0) | -167 | 4 | 13.0 | 0.0 |
| KIHb | 1984 | 4 | 8 | KIHb(66.5)-SASa(69.5) | -97 | 8 | 9.0 | 4.0 |
| KIHb | 1984 | 4 | 7 | KIHb(75.5)-HELb(60.5) | -171 | 5 | 12.0 | 1.0 |
| KIHb | 1984 | 4 | 6 | CINa(56.0)-KIHb(80.0) | -101 | 4 | 13.0 | 1.0 |
| KIHb | 1984 | 4 | 5 | SRMa(48.0)-KIHb(88.0) | -207 | 7 | 10.0 | 1.0 |
| KIHb | 1984 | 4 | 3 | SASa(74.5)-KIHb(61.5) | -154 | 7 | 10.0 | 4.0 |
| KIHb | 1984 | 4 | 2 | HELb(58.0)-KIHb(78.0) | -125 | 3 | 14.0 | 1.0 |
| KIHb | 1984 | 4 | 1 | KIHb(96.0)-KIHc(40.0) | -232 | 5 | 12.0 | 0.0 |
| KIHb | 1983 | 3 | 9 | BORa(86.0)-KIHb(49.0) | -238 | 13 | 4.0 | 8.0 |
| KIHa | 1983 | 1 | 8 | KIHa(76.0)-HELa(60.0) | -145 | 8 | 9.0 | 3.0 |
| KIHb | 1983 | 3 | 7 | KIHb(52.0)-REBa(84.0) | -187 | 9 | 7.0 | 6.0 |
| KIHa | 1983 | 1 | 6 | MJAa(85.5)-KIHa(50.5) | -167 | 15 | 2.0 | 8.0 |
| KIHa | 1983 | 1 | 5 | KIHa(54.0)-MATa(82.0) | -90 | 12 | 5.0 | 7.0 |
| KIHb | 1983 | 3 | 4 | MATb(80.0)-KIHb(55.0) | -204 | 8 | 9.0 | 5.0 |
| KIHb | 1983 | 3 | 3 | KIHb(41.0)-ASSb(95.0) | -118 | 9 | 8.0 | 7.0 |
| KIHb | 1983 | 3 | 2 | RESa(55.5)-KIHb(79.5) | -225 | 10 | 6.5 | 4.0 |
| KIHa | 1983 | 1 | 1 | KIHa(78.0)-SABa(58.0) | -25 | 5 | 12.0 | 2.0 |
| KIHa | 1982 | 1 | 11 | KIHa(68.0)-MJAa(65.0) | -141 | 13 | 4.0 | 6.0 |
| KIHa | 1982 | 1 | 10 | MATa(76.5)-KIHa(59.5) | -97 | 11 | 6.0 | 7.0 |
| KIHa | 1982 | 1 | 9 | KIHa(76.0)-MALa(60.0) | -54 | 10 | 7.0 | 4.0 |
| KIHa | 1982 | 1 | 8 | ASSa(75.0)-KIHa(61.0) | -154 | 14 | 3.0 | 7.0 |
| KIHa | 1982 | 1 | 7 | KIHa(89.0)-LOUa(47.0) | -149 | 10 | 7.0 | 2.0 |
| KIHa | 1982 | 1 | 6 | SABa(74.0)-KIHa(62.0) | -346 | 16 | 1.0 | 8.0 |
| KIHb | 1982 | 2 | 5 | SCBa(72.0)-KIHb(64.0) | -142 | 4 | 13.0 | 2.0 |
| KIHb | 1982 | 2 | 4 | WATb(86.0)-KIHb(50.0) | -139 | 5 | 12.0 | 3.0 |
| KIHb | 1982 | 2 | 3 | KIHb(55.0)-OUEb(81.0) | -218 | 12 | 5.0 | 7.0 |
| KIHb | 1982 | 2 | 2 | KIHb(48.0)-PICa(88.0) | -87 | 4 | 13.0 | 3.0 |
| KIHa | 1982 | 1 | 1 | KIHa(76.0)-PHEa(60.0) | -257 | 15 | 2.0 | 7.0 |
| KIHa | 1981 | 1 | 11 | LEXa(64.0)-KIHa(72.0) | -168 | 14 | 3.0 | 6.0 |
| KIHa | 1981 | 1 | 10 | WATa(75.5)-KIHa(60.5) | -132 | 11 | 5.5 | 5.5 |
| KIHa | 1981 | 1 | 9 | KIHa(50.0)-OUEa(86.0) | -238 | 15 | 2.0 | 8.0 |
| KIHa | 1981 | 1 | 8 | KIHa(69.0)-HELa(67.0) | -130 | 8 | 9.0 | 3.0 |
| KIHa | 1981 | 1 | 7 | PHEa(60.0)-KIHa(76.0) | -53 | 5 | 12.0 | 1.0 |
| KIHa | 1981 | 1 | 6 | MJAa(75.5)-KIHa(60.5) | -206 | 11 | 6.0 | 5.0 |
| KIHa | 1981 | 1 | 5 | KIHa(72.0)-SACa(64.0) | -58 | 5 | 12.0 | 3.0 |
| KIHa | 1981 | 1 | 4 | MALa(70.0)-KIHa(66.0) | -80 | 15 | 2.0 | 8.0 |
| KIHa | 1981 | 1 | 3 | KIHa(80.0)-WATb(56.0) | -179 | 13 | 4.0 | 6.0 |
| KIHa | 1981 | 1 | 2 | LOUa(90.0)-KIHa(46.0) | -161 | 7 | 10.0 | 6.0 |
| KIHa | 1981 | 1 | 1 | KIHa(72.0)-SABa(64.0) | -79 | 7 | 10.0 | 2.0 |
| KIHa | 1980 | 2 | 9 | MJAb(54.0)-KIHa(82.0) | -133 | 5 | 12.0 | 2.0 |
| KIHa | 1980 | 2 | 8 | KIHa(63.5)-MALb(72.5) | -139 | 4 | 13.0 | 2.0 |
| KIHa | 1980 | 2 | 7 | KIHa(79.0)-SCBa(57.0) | -144 | 10 | 7.0 | 4.0 |
| KIHa | 1980 | 2 | 6 | VENa(65.0)-KIHa(71.0) | -225 | 13 | 4.0 | 6.0 |
| KIHa | 1980 | 2 | 5 | KIHa(72.0)-LOUb(64.0) | -95 | 9 | 8.0 | 4.0 |
| KIHa | 1980 | 2 | 4 | KIHa(80.0)-WATb(56.0) | -92 | 5 | 12.0 | 1.0 |
| KIHa | 1980 | 2 | 3 | KIHa(90.0)-LEXb(45.0) | -141 | 8 | 9.0 | 2.0 |
| KIHa | 1980 | 2 | 2 | SALa(51.5)-KIHa(84.5) | -212 | 7 | 10.0 | 2.0 |
| KIHa | 1980 | 2 | 1 | HELa(54.0)-KIHa(82.0) | -96 | 5 | 12.0 | 1.0 |
| KIHa | 1979 | 1 | 9 | WATa(77.5)-KIHa(58.5) | -42 | 2 | 15.0 | 1.0 |
| KIHa | 1979 | 1 | 8 | OUEa(78.0)-KIHa(58.0) | -161 | 12 | 4.5 | 6.0 |
| KIHa | 1979 | 1 | 7 | KIHa(65.0)-SACa(71.0) | -228 | 10 | 7.0 | 4.0 |
| KIHa | 1979 | 1 | 6 | HELa(74.5)-KIHa(61.5) | -117 | 12 | 5.0 | 6.0 |
| KIHa | 1979 | 1 | 5 | KIHa(61.0)-MJAa(75.0) | -53 | 8 | 9.0 | 4.0 |
| KIHa | 1979 | 1 | 4 | KIHa(72.0)-LEXa(64.0) | -230 | 13 | 4.0 | 6.0 |
| KIHa | 1979 | 1 | 3 | LOUa(88.0)-KIHa(48.0) | -154 | 13 | 4.0 | 7.0 |
| KIHa | 1979 | 1 | 2 | KIHa(72.0)-MALa(64.0) | -84 | 1 | 16.0 | 0.0 |
| KIHa | 1979 | 1 | 1 | SABa(99.0)-KIHa(37.0) | -182 | 10 | 6.0 | 8.0 |
| KIHa | 1978 | 2 | 9 | VENa(57.5)-KIHa(78.5) | -130 | 10 | 7.0 | 4.0 |
| KIHa | 1978 | 2 | 8 | KIHa(67.0)-OUEb(69.0) | -217 | 7 | 10.0 | 4.0 |
| KIHa | 1978 | 2 | 7 | SALa(57.0)-KIHa(79.0) | -110 | 8 | 9.0 | 3.0 |
| KIHa | 1978 | 2 | 6 | WATb(48.5)-KIHa(87.5) | -111 | 1 | 16.0 | 0.0 |
| KIHa | 1978 | 2 | 5 | KIHa(69.0)-MALb(67.0) | -228 | 13 | 3.5 | 6.5 |
| KIHa | 1978 | 2 | 2 | KIHa(89.0)-PHEa(47.0) | -127 | 5 | 12.0 | 1.0 |
| KIHa | 1978 | 2 | 1 | KIHa(84.0)-LONa(52.0) | -237 | 6 | 11.0 | 2.0 |
| KIHa | 1977 | 2 | 9 | SACa(56.5)-KIHa(79.5) | -82 | 6 | 11.0 | 2.0 |
| KIHa | 1977 | 2 | 8 | KIHa(85.0)-VENa(51.0) | -222 | 6 | 11.0 | 1.0 |
| KIHa | 1977 | 2 | 7 | LEXb(67.0)-KIHa(69.0) | -156 | 6 | 11.0 | 3.0 |
| KIHa | 1977 | 2 | 6 | KIHa(83.5)-LONa(52.5) | -101 | 10 | 7.0 | 4.0 |
| KIHa | 1977 | 2 | 4 | KIHa(65.0)-MALb(71.0) | -41 | 1 | 16.0 | 0.0 |
| KIHa | 1977 | 2 | 3 | KIHa(87.0)-MJAb(49.0) | -96 | 4 | 13.0 | 1.0 |
| KIHa | 1977 | 2 | 2 | CVLa(42.0)-KIHa(94.0) | -40 | 1 | 16.0 | 0.0 |
| KIHa | 1977 | 2 | 1 | KIHa(78.5)-WARa(57.5) | -267 | 3 | 14.0 | 1.0 |