chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159821200159821201GA14GENIChomozygous71183686
5159823281159823282GT12GENIChomozygous71183688
5159824316159824317TG22GENIChomozygous71183690
5159824412159824413AG5GENIChomozygous71183692
5159824800159824801GA8GENIChomozygous71183694
5159827825159827826CA7GENIChomozygous71183700
5159829565159829566TG19GENIChomozygous71183702
5159830492159830493CT16GENIChomozygous71183704
5159831588159831589CT8GENIChomozygous71183706
5159832014159832015AC11GENIChomozygous71183708
5159832398159832399GC13GENIChomozygous71183710
5159833104159833105GA14GENIChomozygous71183712
5159833177159833178TC8GENIChomozygous71183714
5159833573159833574AG9GENIChomozygous71183716
5159834636159834637CT20GENIChomozygous71183718
5159835176159835177TA16GENIChomozygous71183720
5159835331159835332AG11GENIChomozygous71183722
5159835850159835851GC15GENICpossibly homozygous71183724
5159836101159836102GA11GENICpossibly homozygous71183726
5159836247159836248CT17GENIChomozygous71183728
5159836358159836359TC4GENIChomozygous71183730
5159837366159837367GA4GENIChomozygous71183732
5159837581159837582CG7GENIChomozygous71183734
5159837847159837848GC13GENIChomozygous71183736
5159837869159837870GC12GENIChomozygous71183738
5159838048159838049GA8GENIChomozygous71183740
5159838056159838057CT6GENIChomozygous71183742
5159838213159838214AG10GENIChomozygous71183744
5159838399159838400GA6GENIChomozygous71183746
5159838559159838560TA3GENIChomozygous71183748
5159839185159839186CT13GENIChomozygous71183750
5159839398159839399CT5GENIChomozygous71183752
5159839514159839515AG5GENIChomozygous71183754
5159839525159839526GA8GENIChomozygous71183756