chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1326522613265227TC6GENIChomozygous108228646
X1326536013265361TC10GENIChomozygous108228648
X1326574513265746TC10GENIChomozygous108228650
X1326613613266137TC8GENIChomozygous108228652
X1326615613266157AG15GENIChomozygous108228654
X1326742513267426AG9GENIChomozygous108228656
X1326758713267588TC10GENIChomozygous108228658
X1326842413268425GA13GENIChomozygous108228660
X1327280413272805TG14GENIChomozygous108228666
X1327394813273949GA9GENIChomozygous108228668
X1327472913274730CT13GENIChomozygous108228670
X1327727313277274TC14GENIChomozygous108228672
X1327750013277501GA7GENIChomozygous108228674
X1327837513278376CA17GENIChomozygous108228676
X1327936513279366GT6GENIChomozygous108228678
X1327950013279501GA4GENIChomozygous108228680
X1327977713279778CT6GENIChomozygous108228682
X1328141813281419AG5GENIChomozygous108228684
X1328145513281456AC8GENIChomozygous108228686
X1328187713281878AC10GENIChomozygous108228688
X1328202313282024CA14GENIChomozygous108228692
X1328212513282126GA13GENIChomozygous108228694
X1328124413281245TG8GENIChomozygous108438928