chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76011372960113730TA29GENIChomozygous116369485
76011543760115438CT38GENIChomozygous116369487
76011786060117861TA33GENIChomozygous116176074
76011790760117908TC36GENIChomozygous116369488
76011798260117983CT42GENIChomozygous116369489
76011849060118491CA17GENIChomozygous116369490
76011903660119037CT25GENIChomozygous116369491
76011980560119806TC17GENIChomozygous116176076
76012012360120124TC25GENICpossibly homozygous116176078
76012030360120304CT18GENIChomozygous116176082
76012042260120423TG16GENICpossibly homozygous116176084
76012072460120725TC14GENIChomozygous116369492
76012141660121417TC13GENIChomozygous116369493
76012156460121565AG22GENIChomozygous116369494
76012201760122018GA12GENIChomozygous116369495