chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159821200159821201GA14GENIChomozygous71183686
5159823281159823282GT28GENIChomozygous71183688
5159824316159824317TG21GENIChomozygous71183690
5159824412159824413AG32GENIChomozygous71183692
5159824800159824801GA29GENIChomozygous71183694
5159825581159825582TC1GENIChomozygous71473331
5159827357159827358GA29GENICpossibly homozygous71183698
5159827590159827591TG36GENICheterozygous71473333
5159827825159827826CA18GENIChomozygous71183700
5159829565159829566TG27GENIChomozygous71183702
5159830492159830493CT15GENIChomozygous71183704
5159831588159831589CT29GENIChomozygous71183706
5159832014159832015AC24GENIChomozygous71183708
5159832398159832399GC23GENIChomozygous71183710
5159833104159833105GA12GENIChomozygous71183712
5159833177159833178TC15GENIChomozygous71183714
5159833573159833574AG17GENIChomozygous71183716
5159834636159834637CT14GENIChomozygous71183718
5159835176159835177TA39GENIChomozygous71183720
5159835331159835332AG28GENIChomozygous71183722
5159835850159835851GC20GENICpossibly homozygous71183724
5159836101159836102GA24GENIChomozygous71183726
5159836247159836248CT26GENIChomozygous71183728
5159836358159836359TC28GENIChomozygous71183730
5159837366159837367GA23GENIChomozygous71183732
5159837581159837582CG32GENIChomozygous71183734
5159837847159837848GC26GENIChomozygous71183736
5159837869159837870GC23GENIChomozygous71183738
5159838048159838049GA13GENIChomozygous71183740
5159838056159838057CT14GENICpossibly homozygous71183742
5159838213159838214AG15GENIChomozygous71183744
5159838399159838400GA20GENIChomozygous71183746
5159838559159838560TA16GENIChomozygous71183748
5159839185159839186CT19GENIChomozygous71183750
5159839398159839399CT24GENICpossibly homozygous71183752
5159839514159839515AG22GENIChomozygous71183754
5159839525159839526GA27GENICpossibly homozygous71183756