chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2200520022005201GC26GENIChomozygous140622550
X2200527422005275TC32GENIChomozygous140622551
X2201219522012196TC27GENIChomozygous140622552
X2201294822012949TG20GENIChomozygous140622553
X2201306822013069A24GENIChomozygous140578813
X2201522922015230CT25GENIChomozygous140622554
X2201554422015545GA19GENIChomozygous140622555
X2201611622016116T16GENIChomozygous140578814
X2201747622017477AG22GENIChomozygous140622556
X2201826822018269TC16GENIChomozygous140622557
X2201880222018803T18GENIChomozygous140578815
X2201918322019184A19GENIChomozygous140578816
X2202256722022568AC35GENIChomozygous140622558
X2202293522022935A24GENIChomozygous140578817
X2202339422023395AG27GENIChomozygous140622559
X2202415422024155TA16GENIChomozygous140622560
X2202490622024907CA22GENIChomozygous140622561
X2202574422025750TCCCTC25GENIChomozygous140578818
X2202575622025780TCCTTCTCCCTCTCCCTCTCCCTC26GENIChomozygous140578819
X2202601522026016GA21GENIChomozygous140622562
X2202609722026098AG20GENIChomozygous140622563
X2202671622026717GA23GENIChomozygous140622564