chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116928822116928823AC20GENIChomozygous790181923
7116930571116930572TC33GENIChomozygous790181924
7116930950116930951TC24GENICpossibly homozygous790181925
7116931640116931641TC28GENIChomozygous790181926
7116932522116932523GA21GENIChomozygous790181927
7116932532116932533GA24GENIChomozygous790181928
7116933057116933058AT26GENIChomozygous790181929
7116933972116933973AG31GENIChomozygous790181930
7116934411116934412GA31GENIChomozygous790181931
7116935780116935781GT30GENIChomozygous790181932
7116936326116936327GT23GENICheterozygous790181933
7116937285116937286GT28GENIChomozygous790181934
7116939739116939740TG27GENIChomozygous790181935
7116941317116941318TC25GENIChomozygous790181936
7116941522116941523AG24GENIChomozygous790181937
7116941528116941529TA19GENIChomozygous790181938
7116941529116941530CA19GENIChomozygous790181939
7116941720116941721CA24GENIChomozygous790181940
7116941721116941722TG24GENIChomozygous790181941