chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124810509124810511AT--6GENICheterozygous45267724
X124812323124812324CG16GENIChomozygous45216293
X124812630124812631GA5GENIChomozygous45216294
X124843224124843225AG14GENICheterozygous45216325
X124843254124843255A-11GENICheterozygous45314354
X124843913124843914TTA8GENICheterozygous45216327
X124852133124852135TG--1GENIChomozygous45267728
X124852139124852141GT--1GENIChomozygous45267729
X124852144124852145TC1GENIChomozygous45267730
X124852164124852165T-1GENIChomozygous45216337
X124852168124852169G-1GENIChomozygous45216338
X124852172124852173C-1GENIChomozygous45216339
X124852177124852178T-3GENIChomozygous45216340
X124852182124852183C-3GENIChomozygous45216341
X124852186124852187T-3GENIChomozygous45216342
X124852192124852193T-3GENIChomozygous45216343
X124852199124852200T-3GENIChomozygous45216344
X124852203124852204G-3GENIChomozygous45216345
X124852212124852213T-4GENIChomozygous45216346
X124852217124852218T-5GENIChomozygous45216347
X124852228124852229C-9GENIChomozygous45216348
X124852236124852237T-8GENIChomozygous45216349