chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37991825979918260GT62GENIChomozygous111634794
37991922879919229GA27GENIChomozygous111634795
37991960179919602AT62GENIChomozygous111634796
37991973679919737TC46GENIChomozygous111634797
37991985079919851CA57GENIChomozygous111634798
37992094679920947GT41GENIChomozygous111634799
37992117579921176GA52GENICpossibly homozygous111634800
37992164779921648AG52GENIChomozygous111634801
37992244479922445AG32GENICpossibly homozygous111634802
37992612579926126AG34GENIChomozygous111634803
37992798979927990AG26GENIChomozygous111634804
37992806679928067TA42GENICpossibly homozygous111634805
37992860179928602TC57GENICpossibly homozygous111634806
37992863979928640CT65GENICpossibly homozygous111634807
37992903179929032AG51GENIChomozygous111634808
37992938179929382CG59GENIChomozygous111634809
37992949279929493TC46GENICpossibly homozygous111634810
37992958479929585AG60GENICpossibly homozygous111634811
37992958779929588CT59GENICpossibly homozygous111634812
37992966079929661GA48GENIChomozygous111634813
37992993779929938AG37GENICpossibly homozygous111634814
37993064779930648AG47GENIChomozygous111634815
37993222879932229CT46GENIChomozygous111634816
37993253979932540GC52GENIChomozygous111634817
37993295579932956CT38GENICheterozygous112286792
37993469579934696TG58GENIChomozygous111634818
37993490779934908GA46GENIChomozygous111634819
37993586179935862CT74GENIChomozygous111634820
37993586679935867CG71GENIChomozygous111634821
37993606579936066AG47GENIChomozygous111634822
37993659379936594AG60GENIChomozygous111634823
37993673379936734TC81GENIChomozygous111634824
37993690079936901AG60GENIChomozygous111634825
37993745379937454CT21GENICpossibly homozygous111634826
37993746879937469CG22GENIChomozygous111634827