chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37991825979918260GT24GENIChomozygous111634794
37991973679919737TC22GENIChomozygous111634797
37991985079919851CA21GENIChomozygous111634798
37992094679920947GT15GENIChomozygous111634799
37992164779921648AG21GENIChomozygous111634801
37992244479922445AG9GENIChomozygous111634802
37992158379921584TC26GENIChomozygous112390262
37992357879923579CT21GENIChomozygous112390263
37992560879925609CG7GENIChomozygous131635949
37992612579926126AG14GENIChomozygous111634803
37992679279926792G19GENIChomozygous131624134
37992798979927990AG31GENIChomozygous111634804
37992806679928067TA30GENIChomozygous111634805
37992860179928602TC21GENIChomozygous111634806
37992863979928640CT16GENIChomozygous111634807
37992903179929032AG27GENIChomozygous111634808
37992938179929382CG21GENIChomozygous111634809
37992958479929585AG32GENIChomozygous111634811
37992958779929588CT31GENIChomozygous111634812
37992993779929938AG17GENIChomozygous111634814
37993064779930648AG10GENIChomozygous111634815
37993222879932229CT8GENIChomozygous111634816
37993253979932540GC14GENIChomozygous111634817
37993469579934696TG19GENIChomozygous111634818
37993490779934908GA12GENIChomozygous111634819
37993586179935862CT33GENIChomozygous111634820
37993586679935867CG35GENIChomozygous111634821
37993606579936066AG27GENIChomozygous111634822
37993659379936594AG29GENIChomozygous111634823
37993673379936734TC21GENIChomozygous111634824
37993690079936901AG11GENIChomozygous111634825
37993730079937301TC25GENIChomozygous112390264
37993745379937454CT23GENIChomozygous111634826
37993746879937469CG21GENICpossibly homozygous111634827
37992846579928465AAACA22GENIChomozygous127900247
37993029079930291A19GENIChomozygous127900248
37993281379932814T4GENIChomozygous127900249
37993282879932829G7GENIChomozygous127900250
37993294079932950TGTCTCTGTG15GENIChomozygous127900251
37992810379928104AG36GENIChomozygous120110480