chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75904731859047319AT12GENIChomozygous53930391
75905214059052142AC--12GENICheterozygous54977444
75906325159063252AG7GENIChomozygous53930394
75906325359063254AC6GENIChomozygous53930396
75906325759063258TA6GENIChomozygous53930398
75906325859063259GA6GENIChomozygous53930400
75906326859063269GT5GENIChomozygous53930402
75906327459063275GT6GENIChomozygous53930404
75906328159063282AT6GENIChomozygous53930406
75906329359063294G-6GENIChomozygous53930408
75906331059063311AT3GENIChomozygous53930410
75906331359063314A-3GENIChomozygous53930412
75906331659063317AT3GENIChomozygous54977448
75906331759063318AT3GENIChomozygous54977450
75906332059063321CT3GENIChomozygous54977452
75906332459063325G-3GENIChomozygous53930413
75906332659063327G-3GENIChomozygous53930415
75906333659063337A-3GENIChomozygous53930417
75906333859063339GT3GENIChomozygous54977454
75906334659063347GT2GENIChomozygous54196089
75906334959063350CCTTTTCACTT2GENIChomozygous54977456
75906335459063355GT2GENIChomozygous54977458
75906335859063362GGAA----2GENIChomozygous54977460
75906336959063370AT1GENIChomozygous54977462
75906337459063378GAAG----1GENIChomozygous54977464
75906338759063388GT1GENIChomozygous54977476
75906339159063392GT1GENIChomozygous53930419
75905309559053097TG--13GENICheterozygous55024875