chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2203667873203667874AG29GENICpossibly homozygous111157386
2203668706203668707GA35GENIChomozygous120214668
2203668982203668983TG34GENIChomozygous120214669
2203669980203669981GA54GENIChomozygous120214670
2203670176203670177AG53GENIChomozygous110210704
2203670435203670436AG42GENIChomozygous111157396
2203670703203670704TC39GENIChomozygous111157402
2203670768203670769AG27GENIChomozygous120214671
2203670804203670805AG23GENIChomozygous111157404
2203670814203670815AG24GENIChomozygous111157406
2203670831203670832GA25GENIChomozygous120214672
2203671031203671032GC36GENIChomozygous111157408
2203671286203671287CT38GENIChomozygous111157410
2203671326203671327GC32GENIChomozygous111157414
2203671733203671734GA35GENIChomozygous111157418
2203671934203671935AG27GENIChomozygous110210705
2203671985203671986AG41GENIChomozygous111157420
2203672013203672014AG40GENIChomozygous110210706
2203672337203672338CA51GENICpossibly homozygous110210709
2203672748203672749CT29GENIChomozygous120214673
2203672968203672969CT32GENIChomozygous120214674
2203673289203673290TC41GENIChomozygous120214675
2203673545203673546TA34GENIChomozygous120214676
2203673976203673977TC34GENIChomozygous110210710
2203674025203674026AG40GENIChomozygous110210711
2203674075203674076GA35GENIChomozygous120214677
2203674331203674332TC56GENIChomozygous110210713
2203674454203674455TC37GENIChomozygous110210714
2203675365203675366CT53GENIChomozygous111157424
2203675636203675637TA61GENIChomozygous120214678
2203677017203677018CT36GENIChomozygous120214679
2203677353203677354GA37GENIChomozygous120214680
2203678222203678223AG64GENIChomozygous110210733
2203678635203678636AC55GENIChomozygous110210737
2203678846203678847TG67GENIChomozygous110210740
2203678989203678990TC25GENIChomozygous110210742
2203679463203679464AG33GENICpossibly homozygous110210746
2203679926203679927TC51GENIChomozygous110210748
2203673122203673123CT13GENIChomozygous120394373