chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1654870616548707CT21GENIChomozygous45274440
X1654890416548908TCTA----5GENIChomozygous45501477
X1655216916552170AAT9GENICpossibly homozygous45274441
X1655216916552170AATT9GENICheterozygous45665642
X1655281716552818AG11GENIChomozygous45274442
X1655308216553083TC9GENIChomozygous45274443
X1655531916555320CT12GENIChomozygous45274444
X1655667916556680CT11GENIChomozygous45274445
X1655702016557022AC--3GENIChomozygous45795358
X1655820816558209CCAAA7GENIChomozygous45274447
X1655822016558222CA--7GENIChomozygous45274448
X1655942116559422TC15GENIChomozygous45274449
X1656013816560139AAT6GENIChomozygous45274450
X1656130616561319AAAAAGAAAAAAG-------------9GENIChomozygous45274451
X1656211416562115TTC2GENIChomozygous45274452
X1656212016562121AC1GENIChomozygous45330976
X1656227016562271AG13GENIChomozygous45274453