chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
202973273929732740GC2GENIChomozygous45509613
202973486929734870AG4GENICheterozygous45701667
202973487329734874TC4GENICheterozygous45701668
202973487429734875GA4GENICheterozygous45701669
202973630129736302CT12GENIChomozygous45509621
202973728729737288TC6GENICheterozygous45509623
202973827429738275GA8GENIChomozygous45701671
202973904929739050GT12GENICpossibly homozygous45509625
202973969829739699AAT3GENICheterozygous45509627
202974269729742698AC6GENIChomozygous45822057
202974269929742700CT5GENIChomozygous45822058
202974270129742702AG4GENIChomozygous45805007
202974270629742707TG4GENIChomozygous45701672
202974355829743559GGGAGGAAGATGAGGAGGAGGAAGAA1GENIChomozygous45822059
202974723329747234GA13GENIChomozygous45739758
202974854729748548AC14GENICpossibly homozygous45739759
202975144129751442A-3GENICheterozygous45509644
202975149129751492TC10GENIChomozygous45509646
202975193829751939CA11GENIChomozygous45509648
202975241629752417AATGCTC3GENICheterozygous45509652
202975500629755007CT6GENIChomozygous45739760
202975500729755008CT6GENIChomozygous45739761
202975537629755377AG27GENICpossibly homozygous45509654
202975581229755813CT10GENIChomozygous45509656
202975648629756487AG8GENICheterozygous45509658
202975664129756642TTTA7GENIChomozygous45509660
202975858329758584T-4GENIChomozygous45509664
202975965929759661TT--8GENIChomozygous45509672
202976044729760448TG3GENIChomozygous45509674
202976115329761154GA7GENIChomozygous45962824
202976132929761330AAT6GENICheterozygous45701681
202976167329761674AG22GENIChomozygous45701682
202976477329764774GC4GENIChomozygous45701683
202976508029765081AT5GENICheterozygous45509680
202976526729765268CT10GENICheterozygous45509682