chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75904731859047319AT14GENIChomozygous53930391
75905214059052142AC--7GENICheterozygous54977444
75905647159056472CCTTTTT5GENICheterozygous54977446
75906325159063252AG6GENIChomozygous53930394
75906325359063254AC6GENIChomozygous53930396
75906325759063258TA7GENIChomozygous53930398
75906325859063259GA7GENIChomozygous53930400
75906326859063269GT8GENIChomozygous53930402
75906327459063275GT9GENIChomozygous53930404
75906328159063282AT8GENIChomozygous53930406
75906329359063294G-6GENIChomozygous53930408
75906331059063311AT3GENIChomozygous53930410
75906331359063314A-3GENIChomozygous53930412
75906331659063317AT3GENIChomozygous54977448
75906331759063318AT3GENIChomozygous54977450
75906332059063321CT3GENIChomozygous54977452
75906332459063325G-3GENIChomozygous53930413
75906332659063327G-3GENIChomozygous53930415
75906333659063337A-2GENIChomozygous53930417
75906333859063339GT2GENIChomozygous54977454
75906334659063347GT2GENIChomozygous54196089
75906334959063350CCTTTTCACTT2GENIChomozygous54977456
75906335459063355GT2GENIChomozygous54977458
75906335859063362GGAA----3GENIChomozygous54977460
75906336959063370AT2GENIChomozygous54977462
75906337459063378GAAG----1GENIChomozygous54977464
75906337959063380GT1GENIChomozygous54977466
75906338159063382GT1GENIChomozygous54977468
75906338259063383AT1GENIChomozygous54977470
75906338359063384AT1GENIChomozygous54977472
75906338559063386GT1GENIChomozygous54977474
75906338759063388GT1GENIChomozygous54977476
75906339159063392GT1GENIChomozygous53930419