chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1552883915528840GC16GENIChomozygous108542452
X1553163015531631CG7GENIChomozygous108542454
X1553177615531777AG9GENIChomozygous108233458
X1554060215540603AG12GENIChomozygous108472221
X1554086815540869CT5GENIChomozygous108542456
X1554153315541534GA14GENIChomozygous108233464
X1554177915541780GA9GENIChomozygous108472223
X1554213015542131CT4GENIChomozygous108542458
X1554245415542455CG15GENIChomozygous108233466
X1554302915543030CT9GENIChomozygous108542460
X1554366415543665TC5GENIChomozygous108369878
X1554370315543704CT4GENIChomozygous108472225
X1554394215543943CT10GENIChomozygous108542462
X1554482115544822CT7GENIChomozygous108233472
X1554590815545909AC5GENIChomozygous108233474
X1554613415546135AG4GENICheterozygous125100929
X1554675915546760GA12GENIChomozygous108233476
X1554758515547586CA3GENICheterozygous125159410
X1555027115550272AG6GENIChomozygous108233478
X1555149515551496CA6GENIChomozygous108233480
X1555208315552084CT10GENIChomozygous108233482