chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157581407157581408CT29GENIChomozygous112906692
4157584670157584671TA27GENICheterozygous112906694
4157584722157584723TA26GENICheterozygous112906696
4157586278157586279AG32GENIChomozygous112906698
4157586839157586840CT47GENIChomozygous112906700
4157587009157587010CA45GENIChomozygous112906702
4157587565157587566CT51GENIChomozygous112906704
4157587876157587877AC38GENIChomozygous112906706
4157588993157588994AT54GENICheterozygous112906708
4157589715157589716CT35GENICheterozygous112906710
4157590274157590275TC40GENIChomozygous112906712
4157590667157590668GA12GENIChomozygous113062912
4157591508157591509GA32GENIChomozygous112906714
4157593016157593017AT41GENICpossibly homozygous113062915