chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139351910139351911TC21GENIChomozygous55749477
5139352071139352073CC--24GENIChomozygous55749478
5139352146139352147AG22GENIChomozygous55749479
5139352156139352157AT25GENIChomozygous55749480
5139352566139352567GC20GENIChomozygous55749481
5139353556139353557TC23GENIChomozygous55749482
5139353770139353771TA18GENIChomozygous55749483
5139354115139354117TT--12GENICpossibly homozygous55749484
5139354116139354117T-12GENICheterozygous56064576
5139354211139354212AG18GENIChomozygous55749485
5139354219139354220CT17GENIChomozygous55749486
5139354414139354415AC23GENIChomozygous55749487
5139354416139354417GC24GENIChomozygous55749488
5139354488139354489CT29GENIChomozygous55749489
5139354792139354793CT25GENIChomozygous55749490
5139355117139355118A-21GENIChomozygous55749491
5139355132139355133GT28GENIChomozygous55749492
5139355511139355512CT20GENIChomozygous55749493
5139355816139355817CT15GENIChomozygous55749494
5139355958139355959GGA1GENIChomozygous56553055
5139356001139356002AG8GENIChomozygous55749502
5139356217139356218GGA15GENICpossibly homozygous55749503
5139356552139356553TC23GENIChomozygous55749504
5139356873139356874TA34GENIChomozygous55749505
5139356876139356877CT34GENIChomozygous55749506