chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121120191811201919CT34GENIChomozygous115254782
121120195011201951AG33GENIChomozygous115254784
121120204911202050TC31GENIChomozygous115254786
121120220511202206TC35GENIChomozygous115254788
121120220911202210GA38GENIChomozygous115415264
121120231011202311AG44GENIChomozygous115254790
121120316711203168TC28GENIChomozygous115254792
121120342411203425TG31GENIChomozygous115415266
121120449311204494AG29GENIChomozygous115254794
121120464211204643AG32GENIChomozygous115254796
121120472811204729AG34GENIChomozygous115254798
121120474111204742TC33GENIChomozygous115254800
121120521711205218TG35GENIChomozygous115254802
121120563611205637TG27GENIChomozygous115254804
121120632511206326AG27GENICpossibly homozygous115437335
121120698311206984TC26GENICpossibly homozygous115254808
121120791211207913CT34GENIChomozygous115254812
121120844811208449AG7GENIChomozygous115254814
121120864211208643CT9GENIChomozygous115254816
121120871711208718TC12GENIChomozygous115254818
121120874211208743TC11GENIChomozygous115254820
121120953211209533TC28GENIChomozygous115254824
121120965711209658TC11GENIChomozygous115254826
121121053211210533TC26GENIChomozygous115254828
121121115311211154CT28GENIChomozygous115254830
121121136211211363GA23GENIChomozygous115254832
121121149311211494GT19GENIChomozygous115254834
121121153011211531TC10GENIChomozygous115361393
121121155811211559GA10GENIChomozygous115254836
121121158911211590TC11GENIChomozygous115254838
121121174611211747GA19GENIChomozygous115254840
121121203511212036CT25GENIChomozygous115254842
121121207611212077AG26GENIChomozygous115437336
121121232611212327AG24GENIChomozygous115254844
121121341111213412GA33GENIChomozygous115254852
121121371411213715TC23GENIChomozygous115415278
121121371511213716GA23GENIChomozygous115415280