chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4077649140776492AT2GENIChomozygous568204412
X4078266640782667AG13GENIChomozygous565395426
X4078861340788614TTGA2GENICheterozygous710578832
X4078866140788663GA--5GENICheterozygous710578833
X4080010540800106T-4GENICheterozygous710578836
X4082123040821231TTG8GENICheterozygous710578838
X4083551640835517AT1GENIChomozygous568204413
X4083551840835519AC1GENIChomozygous568204414
X4083671440836715GGACACACAC9GENICheterozygous710578841
X4083671540836719ACAC----9GENICheterozygous710578839
X4083671740836719AC--9GENICheterozygous710578840
X4086643540866436TTTGTGTGTGTGTGTGTGTGTGTGTGTGTG2GENICheterozygous710578844
X4087556540875566GT8GENIChomozygous568204415
X4087556740875568C-9GENIChomozygous710578845
X4087568840875689GA10GENIChomozygous565395427
X4087569640875697TA11GENIChomozygous565395428
X4087569840875699AT11GENIChomozygous565395429
X4087678240876784GT--3GENICheterozygous710578847
X4088391340883914GGTT3GENICheterozygous710578851
X4089542340895424T-6GENICheterozygous710578852
X4090143640901437CCTGTGTG1GENIChomozygous710578855
X4090327140903272A-15GENIChomozygous710578856
X4093228340932284AAGTT9GENIChomozygous710578857
X4094140040941401TC13GENIChomozygous568204416
X4094140740941408AAC13GENIChomozygous710578858
X4096255540962557CA--9GENICheterozygous710578859
X4096906140969062CCT1GENIChomozygous710578861
X4097461040974611TC3GENIChomozygous568204417
X4099425940994260CT16GENIChomozygous565395430
X4099426240994263CT15GENIChomozygous565395431
X4101723241017233GT8GENIChomozygous565395432
X4101725641017257GT7GENIChomozygous565395433
X4101725741017258AAACAC7GENIChomozygous710578862
X4101726141017265CTTT----6GENIChomozygous710578863
X4101728041017281CCT7GENIChomozygous710578864
X4101731541017316C-7GENIChomozygous710578865