chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227052063227052064GT15GENICheterozygous61105176
1227052132227052133AG15GENICheterozygous61105177
1227052161227052162TC17GENICheterozygous61105178
1227052456227052457AG13GENICheterozygous61105179
1227053226227053227TG19GENICheterozygous61105182
1227053481227053482TC16GENICheterozygous61105183
1227054276227054277AG24GENICheterozygous61105184
1227054307227054308TC22GENICheterozygous61105185
1227054702227054703CA14GENICheterozygous61105186
1227054824227054825T-11GENICheterozygous61105187
1227054848227054849T-10GENICheterozygous61105188
1227054862227054863CT11GENICheterozygous61105189
1227056560227056561CT19GENICheterozygous61105190
1227056646227056647AG17GENICheterozygous61105191
1227056865227056866CT22GENICheterozygous61105192
1227057105227057106CCT12GENICheterozygous61105193
1227057578227057579CG15GENICheterozygous61105197
1227059813227059814CT13GENICheterozygous61105199
1227060252227060253GA15GENICheterozygous61105200
1227060697227060698CA17GENICheterozygous61105201
1227060713227060714GT21GENICheterozygous61105202
1227060832227060833GC21GENICheterozygous61105203
1227060931227060932TC16GENICheterozygous61105204
1227061388227061389AG16GENICheterozygous61105205
1227061763227061764TC16GENICheterozygous61105206
1227062085227062086TTG18GENICheterozygous61105207
1227062103227062104GA21GENICheterozygous61105208
1227065309227065310GC14GENICheterozygous61105210
1227065396227065397AT22GENICheterozygous61105211
1227066147227066148TC7GENICheterozygous61105212
1227067008227067009CA18GENICheterozygous61105215