chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191138983511389836CG44GENICpossibly homozygous109636570
191138993511389936TG35GENICpossibly homozygous109636572
191138995411389955TG34GENICpossibly homozygous109636574
191139050611390507GA46GENIChomozygous119688554
191139211711392118TC71GENICheterozygous119596649
191139215411392155CT82GENICheterozygous119596652
191139428911394290TC17GENICheterozygous119596655
191140211211402113GC25GENIChomozygous109995136
191139716311397164TG47GENIChomozygous109995131
191139835311398354CT16GENIChomozygous109887088
191139836111398362AT15GENIChomozygous109887090
191139836811398369CT13GENIChomozygous109887092
191139838111398382AT9GENIChomozygous109887094
191140310011403101CT61GENIChomozygous109995138
191140482811404829GT54GENICpossibly homozygous109995140
191140483011404831GC53GENICpossibly homozygous109995142
191140700111407002AG32GENIChomozygous109995144
191140808211408083CT58GENIChomozygous109995146
191140953111409532AG64GENICpossibly homozygous109995148
191141024611410247CT48GENIChomozygous109995149
191141038511410386TG48GENICpossibly homozygous109995151
191141164611411647AG47GENIChomozygous109636578
191141264111412642TC45GENIChomozygous109995153
191141312411413125GA55GENIChomozygous109995155
191141452411414525GA56GENICheterozygous119688560
191141474911414750AT49GENICheterozygous119688561
191141475511414756CT49GENICheterozygous119688562
191141477411414775AT49GENICheterozygous119688563
191141592811415929GT46GENICpossibly homozygous109995159
191141614311416144TC61GENIChomozygous109995161
191141618111416182CT54GENIChomozygous109995163
191141624111416242CG36GENIChomozygous109995165
191141805511418056CT32GENIChomozygous109995167
191141822311418224AG50GENIChomozygous109995169
191141863311418634GC53GENIChomozygous109995171
191141962611419627TC39GENIChomozygous109995173
191141693911416940GT54GENIChomozygous110005539
191141859211418593CT48GENIChomozygous110005541