chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X123910636123910637CT8GENIChomozygous45362460
X123910729123910730CG8GENIChomozygous45215164
X123913077123913078AT4GENICheterozygous45362465
X123914006123914007TC3GENIChomozygous45362467
X123914552123914553GA6GENIChomozygous45362468
X123916200123916201TC10GENIChomozygous45215179
X123916919123916920A-2GENIChomozygous45215181
X123918814123918815GA11GENIChomozygous45215187
X123922244123922245GA7GENIChomozygous45362470
X123924654123924655GA4GENIChomozygous45362472
X123925097123925098TC11GENICheterozygous45215206