chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148635856886358569AG9GENICheterozygous118704063
148636047786360478TC21GENIChomozygous113501868
148636176186361762AT22GENIChomozygous114166429
148636200686362007TC15GENIChomozygous113912081
148638058486380585AG2GENIChomozygous118704069
148639481486394815TC15GENIChomozygous113501870
148641652086416521GT14GENIChomozygous113501874
148641656686416567GT11GENIChomozygous118704070
148641669586416696GT6GENIChomozygous118704071
148641669986416700AT6GENIChomozygous118704072
148641675486416755GT9GENIChomozygous118704073
148641675586416756GT9GENIChomozygous118704074
148644485786444858TA16GENIChomozygous113501876
148644488886444889AT18GENIChomozygous113501884
148645161786451618CA18GENICpossibly homozygous118704078
148646247086462471CG59GENICheterozygous118786464
148646247386462474AG57GENICheterozygous118786465
148646247886462479CG60GENICheterozygous118786466
148646398086463981AG108GENICheterozygous118786467
148646398386463984CT106GENICheterozygous118786468
148646402686464027AG130GENICheterozygous118786469
148646412186464122AT160GENICheterozygous118786470
148646415586464156AG188GENICheterozygous118786471
148646416286464163CT169GENICheterozygous118786472
148655327986553280CG5GENIChomozygous118704090