chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170621799170621800CT46GENIChomozygous60941109
1170622348170622349AG36GENIChomozygous60941110
1170622505170622517ACACACACACAC------------8GENIChomozygous62369338
1170622756170622757TC65GENIChomozygous60941111
1170623122170623123CA44GENIChomozygous60941112
1170623441170623442GA31GENIChomozygous60941113
1170624336170624337TTCACACACACACA16GENIChomozygous62173309
1170626767170626771ACAC----3GENIChomozygous62173311
1170628709170628710AG41GENIChomozygous60941115
1170629075170629076GGAA35GENICpossibly homozygous60941116
1170629075170629076GGA35GENICheterozygous62313534
1170629637170629638GA53GENIChomozygous60941117
1170631445170631446TC33GENIChomozygous60941118
1170631481170631482C-36GENIChomozygous60941120
1170632202170632203TC45GENIChomozygous60941121