chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116928822116928823AC45GENIChomozygous775960001
7116930571116930572TC55GENIChomozygous775960002
7116930950116930951TC48GENIChomozygous775960003
7116931640116931641TC43GENIChomozygous775960004
7116932522116932523GA59GENIChomozygous775960005
7116932532116932533GA59GENIChomozygous775960006
7116933057116933058AT49GENIChomozygous775960007
7116933972116933973AG46GENIChomozygous775960008
7116934411116934412GA45GENIChomozygous775960009
7116935780116935781GT37GENIChomozygous775960010
7116937285116937286GT56GENIChomozygous775960011
7116939739116939740TG50GENIChomozygous775960012
7116941317116941318TC62GENICpossibly homozygous775960013
7116941522116941523AG63GENIChomozygous775960014
7116941528116941529TA58GENIChomozygous775960015
7116941529116941530CA58GENIChomozygous775960016
7116941720116941721CA42GENIChomozygous775960017
7116941721116941722TG41GENIChomozygous775960018