chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9113579351113579352GC84GENICheterozygous120284681
9113579360113579361TC92GENICheterozygous117631171
9113579722113579723GT100GENICheterozygous120284682
9113579426113579427TA92GENICheterozygous117427215
9113579428113579429CT93GENICheterozygous117427216
9113579576113579577GC71GENICheterozygous117777180
9113579651113579652CA71GENICheterozygous117777182
9113579721113579722CT98GENICheterozygous117900079
9113579830113579831GC233GENICheterozygous117427220
9113580146113580147CA133GENICheterozygous117631179
9113580147113580148CA133GENICheterozygous117427221
9113580153113580154AT131GENICheterozygous117427222
9113580229113580230AT120GENICheterozygous117427223
9113580239113580240GA117GENICheterozygous117631181
9113580256113580257GA110GENICheterozygous117427224
9113580265113580266GC111GENICheterozygous117427225
9113580345113580346GT50GENICheterozygous117427226
9113580355113580356AC58GENICheterozygous117427227
9113585063113585064AG30GENICheterozygous117427229
9113588131113588132GA51GENIChomozygous117645423
9113580601113580602CT45GENIChomozygous117645420
9113585167113585168CT71GENIChomozygous117645421
9113587986113587987AG68GENICpossibly homozygous117645422
9113590798113590799GA49GENIChomozygous117645424
9113590838113590839GA41GENIChomozygous117645425
9113591342113591343CT26GENIChomozygous117645426
9113591817113591818CT46GENIChomozygous117645427
9113592821113592822TC18GENIChomozygous117427237
9113593424113593425CA46GENICpossibly homozygous117645428
9113594349113594350CT43GENIChomozygous117645429
9113594383113594384TC49GENIChomozygous117645430
9113596280113596281GA50GENIChomozygous117645431
9113596836113596837TC43GENIChomozygous117645432
9113597415113597416CT27GENIChomozygous117427243