chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159821194159821195G14GENICheterozygous72693935
5159821195159821196TC12GENIChomozygous72693938
5159821200159821201GA13GENIChomozygous71183686
5159823281159823282GT16GENICheterozygous71183688
5159824316159824317TG33GENIChomozygous71183690
5159824412159824413AG16GENIChomozygous71183692
5159824800159824801GA7GENIChomozygous71183694
5159827825159827826CA6GENIChomozygous71183700
5159830492159830493CT18GENIChomozygous71183704
5159831588159831589CT24GENIChomozygous71183706
5159832014159832015AC25GENIChomozygous71183708
5159832398159832399GC19GENIChomozygous71183710
5159833104159833105GA18GENIChomozygous71183712
5159833177159833178TC29GENIChomozygous71183714
5159833573159833574AG26GENIChomozygous71183716
5159834636159834637CT10GENIChomozygous71183718
5159835176159835177TA25GENIChomozygous71183720
5159835331159835332AG28GENIChomozygous71183722
5159835850159835851GC7GENIChomozygous71183724
5159836101159836102GA20GENIChomozygous71183726
5159836247159836248CT13GENIChomozygous71183728
5159836358159836359TC14GENIChomozygous71183730
5159835908159835909AG9GENIChomozygous72313247
5159832870159832870A5GENIChomozygous73317293
5159837197159837197AG25GENICheterozygous73317295
5159837366159837367GA11GENIChomozygous71183732
5159837847159837848GC21GENIChomozygous71183736
5159837869159837870GC12GENIChomozygous71183738
5159838048159838049GA4GENIChomozygous71183740
5159838056159838057CT11GENIChomozygous71183742
5159838213159838214AG9GENIChomozygous71183744
5159838399159838400GA17GENIChomozygous71183746
5159839185159839186CT30GENIChomozygous71183750
5159839398159839399CT21GENIChomozygous71183752
5159839514159839515AG18GENIChomozygous71183754
5159839525159839526GA11GENIChomozygous71183756