chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1256962135256962136T19GENIChomozygous131267020
1256962140256962146CCCCCA19GENIChomozygous131267021
1256976234256976235TC21GENIChomozygous108623002
1256979947256979947A14GENIChomozygous131267022
1256981009256981009C17GENIChomozygous131267023
1256962345256962346TA18GENIChomozygous109024265
1256966278256966279CT11GENIChomozygous109024266
1256973800256973801GA17GENIChomozygous109024268
1256981484256981484T5GENIChomozygous127505731
1256972457256972458CG26GENIChomozygous120605294
1256977954256977955GA20GENIChomozygous120605296
1256978856256978857GA24GENIChomozygous120605298
1256990438256990439TA22GENICpossibly homozygous108623012
1256995198256995202AAAG19GENIChomozygous131267025