chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3150588384150588385GT19INTERGENIChomozygous58563484
3150588436150588437GA28INTERGENICpossibly homozygous58563485
3150588937150588938TC28INTERGENICheterozygous57737382
3150589513150589514TG11INTERGENIChomozygous58230450
3150589789150589790TC13INTERGENICpossibly homozygous58563487
3150590016150590017CG14INTERGENIChomozygous58230464
3150590507150590508GA15INTERGENIChomozygous58563488
3150590771150590772CT11INTERGENIChomozygous58563489
3150590943150590944GC5INTERGENIChomozygous58230473
3150592073150592074GA12INTERGENIChomozygous58563490
3150592430150592431AG13INTERGENIChomozygous58230479
3150592806150592807AG16INTERGENIChomozygous58230482
3150593204150593205CT11INTERGENIChomozygous58563491
3150593252150593253CCTTT7INTERGENIChomozygous58563492
3150593815150593816TA17INTERGENIChomozygous58230485
3150593946150593947AG17INTERGENIChomozygous58230486
3150594374150594375TA31INTERGENICheterozygous57737428
3150594375150594376TA31INTERGENICheterozygous57737430
3150596375150596377AC--2GENIChomozygous58654617
3150589352150589358ACACAA------7INTERGENICheterozygous58654612
3150589354150589358ACAA----5INTERGENICheterozygous58654614
3150594077150594078GGCTTTT12INTERGENIChomozygous58654615
3150596810150596811A-8GENICpossibly homozygous57737454
3150597083150597084A-11GENIChomozygous57737472
3150597146150597148AA--15GENIChomozygous58230497
3150597300150597301CCT22GENICpossibly homozygous57737490
3150597328150597329GT24GENICpossibly homozygous58563493