chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31131769411317695GT15GENIChomozygous111875644
31132020211320203TA22GENIChomozygous111446664
31132049111320492TC21GENIChomozygous111446668
31132240611322407CA36GENIChomozygous111875646
31132253611322537TC27GENIChomozygous111446670
31132552211325523GA25GENIChomozygous111446676
31132824911328250TC29GENIChomozygous111446678
31132875111328752TC36GENIChomozygous111446680
31132915711329158AG41GENIChomozygous111446682
31132943211329433AG17GENIChomozygous111446686
31132948711329488GA20GENICpossibly homozygous111875648
31133101411331015GT38GENIChomozygous111446694
31133127711331278AG32GENIChomozygous111446696
31133170711331708AG32GENIChomozygous111446698
31133185211331853GA21GENIChomozygous111446700
31133216711332168TG41GENIChomozygous111446702
31133219311332194TC33GENIChomozygous111446704
31133280011332801AG45GENICpossibly homozygous111446706
31133492811334929GA31GENIChomozygous111875650
31133517211335173CA26GENIChomozygous111875652
31133541911335420AG39GENIChomozygous111446712
31133737111337372CT21GENIChomozygous111875654