chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37991825979918260GT39GENIChomozygous111634794
37991922879919229GA44GENIChomozygous111634795
37991960179919602AT52GENIChomozygous111634796
37991973679919737TC67GENIChomozygous111634797
37991985079919851CA50GENIChomozygous111634798
37992094679920947GT41GENIChomozygous111634799
37992117579921176GA39GENIChomozygous111634800
37992164779921648AG57GENIChomozygous111634801
37992244479922445AG33GENIChomozygous111634802
37992612579926126AG41GENIChomozygous111634803
37992798979927990AG39GENIChomozygous111634804
37992806679928067TA36GENIChomozygous111634805
37992810379928104AG34GENIChomozygous120110480
37992949279929493TC26GENIChomozygous111634810
37992860179928602TC24GENIChomozygous111634806
37992863979928640CT29GENIChomozygous111634807
37992903179929032AG38GENIChomozygous111634808
37992938179929382CG29GENIChomozygous111634809
37992958479929585AG48GENIChomozygous111634811
37992958779929588CT50GENIChomozygous111634812
37992966079929661GA46GENIChomozygous111634813
37992993779929938AG45GENIChomozygous111634814
37993064779930648AG48GENIChomozygous111634815
37993222879932229CT49GENIChomozygous111634816
37993253979932540GC42GENIChomozygous111634817
37993294079932950TGTCTCTGTG24GENIChomozygous127900251
37992846579928465AAACA25GENICpossibly homozygous127900247
37993029079930291A46GENIChomozygous127900248
37993281379932814T13GENIChomozygous127900249
37993282879932829G13GENIChomozygous127900250
37993469579934696TG60GENIChomozygous111634818
37993490779934908GA42GENIChomozygous111634819
37993586179935862CT60GENIChomozygous111634820
37993586679935867CG59GENIChomozygous111634821
37993606579936066AG54GENIChomozygous111634822
37993659379936594AG52GENIChomozygous111634823
37993673379936734TC55GENIChomozygous111634824
37993690079936901AG42GENIChomozygous111634825
37993745379937454CT53GENIChomozygous111634826
37993746879937469CG64GENIChomozygous111634827