chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124812323124812324CG5GENIChomozygous45216293
X124812630124812631GA3GENIChomozygous45216294
X124814962124814963A-6GENICheterozygous45216295
X124850857124850858CCA4GENICheterozygous45216334
X124852139124852141GT--1GENIChomozygous45267729
X124852144124852145TC1GENIChomozygous45267730
X124852155124852156G-1GENIChomozygous45551822
X124852158124852160GC--1GENIChomozygous45551824
X124852164124852165T-1GENIChomozygous45216337
X124852168124852169G-1GENIChomozygous45216338
X124852186124852187T-2GENIChomozygous45216342
X124852147124852151CGGC----1GENIChomozygous45651682
X124852172124852173C-1GENIChomozygous45216339
X124852177124852178T-1GENIChomozygous45216340
X124852182124852183C-1GENIChomozygous45216341
X124852192124852193T-2GENIChomozygous45216343
X124852199124852200T-3GENIChomozygous45216344
X124852203124852204G-4GENIChomozygous45216345
X124852212124852213T-3GENIChomozygous45216346
X124852217124852218T-3GENIChomozygous45216347
X124852228124852229C-7GENIChomozygous45216348
X124852236124852237T-9GENIChomozygous45216349