chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3150588436150588437GA33INTERGENICpossibly homozygous58563485
3150588937150588938TC32INTERGENICheterozygous57737382
3150589352150589358ACACAA------6INTERGENIChomozygous58654612
3150589513150589514TG23INTERGENIChomozygous58230450
3150589542150589543CG27INTERGENIChomozygous59636756
3150590016150590017CG25INTERGENIChomozygous58230464
3150590379150590380CA21INTERGENIChomozygous59636758
3150590507150590508GA15INTERGENIChomozygous58563488
3150590943150590944GC14INTERGENIChomozygous58230473
3150592430150592431AG23INTERGENIChomozygous58230479
3150592806150592807AG20INTERGENIChomozygous58230482
3150593204150593205CT25INTERGENICpossibly homozygous58563491
3150593252150593253CCT24INTERGENICpossibly homozygous57737416
3150593815150593816TA24INTERGENICpossibly homozygous58230485
3150593946150593947AG17INTERGENIChomozygous58230486
3150594077150594078GGCTTTT12INTERGENIChomozygous58654615
3150594374150594375TA34INTERGENICheterozygous57737428
3150594375150594376TA34INTERGENICheterozygous57737430
3150596375150596377AC--6GENIChomozygous58654617
3150596810150596811A-8GENICheterozygous57737454
3150597083150597084A-6GENIChomozygous57737472
3150597146150597148AA--13GENIChomozygous58230497
3150597300150597301CCT15GENIChomozygous57737490
3150597328150597329GT28GENICpossibly homozygous58563493