chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157581407157581408CT44GENIChomozygous112906692
4157584722157584723TA30GENICheterozygous112906696
4157586278157586279AG49GENICpossibly homozygous112906698
4157586839157586840CT67GENIChomozygous112906700
4157587009157587010CA73GENIChomozygous112906702
4157587565157587566CT54GENIChomozygous112906704
4157587876157587877AC39GENIChomozygous112906706
4157588993157588994AT71GENICpossibly homozygous112906708
4157589715157589716CT46GENICheterozygous112906710
4157590274157590275TC61GENIChomozygous112906712
4157590667157590668GA22GENICpossibly homozygous113062912
4157591508157591509GA58GENIChomozygous112906714
4157593016157593017AT55GENICpossibly homozygous113062915