chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31131769411317695GT33GENICpossibly homozygous111875644
31132020211320203TA54GENICpossibly homozygous111446664
31132049111320492TC51GENIChomozygous111446668
31132240611322407CA74GENIChomozygous111875646
31132253611322537TC73GENIChomozygous111446670
31132552211325523GA52GENIChomozygous111446676
31132824911328250TC47GENIChomozygous111446678
31132875111328752TC62GENIChomozygous111446680
31132915711329158AG53GENIChomozygous111446682
31132943211329433AG47GENIChomozygous111446686
31132948711329488GA33GENICheterozygous111875648
31133101411331015GT65GENICpossibly homozygous111446694
31133127711331278AG60GENIChomozygous111446696
31133170711331708AG65GENIChomozygous111446698
31133185211331853GA63GENIChomozygous111446700
31133216711332168TG56GENICpossibly homozygous111446702
31133219311332194TC46GENIChomozygous111446704
31133280011332801AG48GENIChomozygous111446706
31133492811334929GA48GENIChomozygous111875650
31133517211335173CA65GENIChomozygous111875652
31133541911335420AG54GENIChomozygous111446712
31133737111337372CT56GENICpossibly homozygous111875654