chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75904731859047319AT13GENIChomozygous53930391
75905213859052142ACAC----4GENICheterozygous55275771
75905214059052142AC--4GENICheterozygous54977444
75905309559053097TG--18GENICheterozygous55024875
75905647159056472CCTTTTT12GENICheterozygous54977446
75905647159056472CCTTTTCTTTTCT12GENICheterozygous55058514
75906325159063252AG12GENIChomozygous53930394
75906325359063254AC12GENIChomozygous53930396
75906325759063258TA11GENIChomozygous53930398
75906325859063259GA10GENIChomozygous53930400
75906326859063269GT13GENIChomozygous53930402
75906327459063275GT14GENIChomozygous53930404
75906328159063282AT12GENIChomozygous53930406
75906329359063294G-11GENIChomozygous53930408
75906331059063311AT8GENIChomozygous53930410
75906331359063314A-8GENIChomozygous53930412
75906331659063317AT8GENIChomozygous54977448
75906331759063318AT8GENIChomozygous54977450
75906332059063321CT8GENIChomozygous54977452
75906332459063325G-8GENIChomozygous53930413
75906332659063327G-8GENIChomozygous53930415
75906333659063337A-7GENIChomozygous53930417
75906333859063339GT5GENIChomozygous54977454
75906334659063347GT3GENIChomozygous54196089
75906334959063350CCTTTTCACTT3GENIChomozygous54977456
75906335459063355GT3GENIChomozygous54977458
75906335859063362GGAA----3GENIChomozygous54977460
75906337459063378GAAG----1GENIChomozygous54977464
75906337959063380GT1GENIChomozygous54977466
75906338159063382GT2GENIChomozygous54977468
75906338259063383AT2GENIChomozygous54977470
75906338359063384AT2GENIChomozygous54977472
75906338559063386GT3GENIChomozygous54977474
75906338759063388GT4GENIChomozygous54977476
75906339159063392GT4GENIChomozygous53930419
75906368559063686TTACAC8GENIChomozygous55174984