chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159821200159821201GA30GENIChomozygous71183686
5159823281159823282GT33GENIChomozygous71183688
5159824316159824317TG49GENIChomozygous71183690
5159824412159824413AG47GENIChomozygous71183692
5159824800159824801GA37GENIChomozygous71183694
5159827825159827826CA17GENIChomozygous71183700
5159829565159829566TG60GENIChomozygous71183702
5159830492159830493CT21GENIChomozygous71183704
5159831588159831589CT44GENIChomozygous71183706
5159832014159832015AC40GENIChomozygous71183708
5159832398159832399GC34GENIChomozygous71183710
5159833104159833105GA43GENIChomozygous71183712
5159833177159833178TC41GENIChomozygous71183714
5159833573159833574AG50GENIChomozygous71183716
5159834636159834637CT64GENIChomozygous71183718
5159835176159835177TA64GENIChomozygous71183720
5159835331159835332AG48GENIChomozygous71183722
5159835850159835851GC43GENICheterozygous71183724
5159834795159834796AC15GENICheterozygous80841113
5159836101159836102GA60GENIChomozygous71183726
5159836247159836248CT69GENIChomozygous71183728
5159836358159836359TC41GENIChomozygous71183730
5159837366159837367GA35GENICpossibly homozygous71183732
5159837581159837582CG26GENIChomozygous71183734
5159837847159837848GC35GENIChomozygous71183736
5159838213159838214AG46GENIChomozygous71183744
5159837869159837870GC41GENIChomozygous71183738
5159838048159838049GA68GENIChomozygous71183740
5159838056159838057CT62GENIChomozygous71183742
5159838399159838400GA69GENIChomozygous71183746
5159838559159838560TA25GENIChomozygous71183748
5159839185159839186CT39GENIChomozygous71183750
5159839398159839399CT56GENIChomozygous71183752
5159839514159839515AG64GENIChomozygous71183754
5159839525159839526GA58GENIChomozygous71183756