chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2200520022005201GC10GENIChomozygous140622550
X2200527422005275TC10GENIChomozygous140622551
X2201219522012196TC7GENIChomozygous140622552
X2201294822012949TG6GENIChomozygous140622553
X2201306822013069A7GENIChomozygous140578813
X2201522922015230CT5GENIChomozygous140622554
X2201554422015545GA8GENIChomozygous140622555
X2201611622016116T4GENIChomozygous140578814
X2201747622017477AG6GENIChomozygous140622556
X2201826822018269TC7GENIChomozygous140622557
X2201880222018803T12GENIChomozygous140578815
X2201918322019184A5GENIChomozygous140578816
X2202256722022568AC4GENIChomozygous140622558
X2202293522022935A5GENIChomozygous140578817
X2202339422023395AG11GENIChomozygous140622559
X2202415422024155TA7GENIChomozygous140622560
X2202490622024907CA8GENIChomozygous140622561
X2202574422025750TCCCTC8GENIChomozygous140578818
X2202575622025780TCCTTCTCCCTCTCCCTCTCCCTC8GENIChomozygous140578819
X2202601522026016GA10GENIChomozygous140622562
X2202609722026098AG10GENIChomozygous140622563
X2202671622026717GA12GENIChomozygous140622564