chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1326315513263156GA10GENIChomozygous108228644
X1326522613265227TC19GENIChomozygous108228646
X1326536013265361TC14GENIChomozygous108228648
X1326574513265746TC12GENIChomozygous108228650
X1326613613266137TC12GENIChomozygous108228652
X1326615613266157AG11GENIChomozygous108228654
X1326742513267426AG10GENIChomozygous108228656
X1326842413268425GA13GENIChomozygous108228660
X1327207513272076GA6GENIChomozygous108228662
X1327251813272519GC10GENIChomozygous108228664
X1327280413272805TG10GENIChomozygous108228666
X1327394813273949GA10GENIChomozygous108228668
X1327472913274730CT11GENIChomozygous108228670
X1327727313277274TC16GENIChomozygous108228672
X1327750013277501GA7GENIChomozygous108228674
X1327837513278376CA11GENIChomozygous108228676
X1327936513279366GT13GENIChomozygous108228678
X1327950013279501GA10GENIChomozygous108228680
X1327977713279778CT7GENIChomozygous108228682
X1328141813281419AG9GENIChomozygous108228684
X1328187713281878AC11GENIChomozygous108228688
X1328196113281962GT12GENIChomozygous108228690
X1328202313282024CA10GENIChomozygous108228692
X1328212513282126GA16GENIChomozygous108228694