chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159823281159823282GT13GENIChomozygous71183688
5159824316159824317TG35GENIChomozygous71183690
5159824412159824413AG22GENIChomozygous71183692
5159824800159824801GA26GENIChomozygous71183694
5159827357159827358GA14GENIChomozygous71183698
5159827825159827826CA8GENIChomozygous71183700
5159829565159829566TG7GENIChomozygous71183702
5159830492159830493CT14GENIChomozygous71183704
5159831588159831589CT24GENIChomozygous71183706
5159832014159832015AC17GENIChomozygous71183708
5159832398159832399GC16GENIChomozygous71183710
5159833104159833105GA18GENIChomozygous71183712
5159833177159833178TC18GENIChomozygous71183714
5159833573159833574AG14GENIChomozygous71183716
5159834636159834637CT25GENIChomozygous71183718
5159835176159835177TA24GENIChomozygous71183720
5159835331159835332AG35GENIChomozygous71183722
5159835850159835851GC18GENIChomozygous71183724
5159836101159836102GA30GENIChomozygous71183726
5159836247159836248CT21GENIChomozygous71183728
5159836358159836359TC27GENIChomozygous71183730
5159837366159837367GA15GENIChomozygous71183732
5159837581159837582CG5GENIChomozygous71183734
5159837847159837848GC32GENIChomozygous71183736
5159837869159837870GC33GENIChomozygous71183738
5159838048159838049GA25GENIChomozygous71183740
5159838056159838057CT23GENIChomozygous71183742
5159838213159838214AG22GENIChomozygous71183744
5159838399159838400GA27GENIChomozygous71183746
5159838559159838560TA4GENIChomozygous71183748
5159839185159839186CT34GENICpossibly homozygous71183750
5159839398159839399CT29GENIChomozygous71183752
5159839514159839515AG24GENIChomozygous71183754
5159839525159839526GA21GENIChomozygous71183756
5159834310159834311AT7GENIChomozygous72461639
5159827359159827360AG15GENICpossibly homozygous72313243
5159831052159831053GT4GENIChomozygous72313245
5159835908159835909AG12GENIChomozygous72313247
5159832801159832802AG3GENIChomozygous72577603
5159834302159834303TG3GENIChomozygous72577605
5159834307159834308GT3GENIChomozygous72577607