chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113169465431694655TC31GENIChomozygous115812390
113169481331694814GT29GENIChomozygous115812392
113169570831695709AG47GENICpossibly homozygous115812394
113169629431696295CG41GENIChomozygous115812396
113169633031696331TC33GENIChomozygous116035374
113169656231696563TC17GENIChomozygous116351621
113169675731696758AG49GENICpossibly homozygous116035376
113169722031697221CT35GENIChomozygous116035378
113169739331697394AG44GENIChomozygous115812400
113169776731697768AT31GENIChomozygous116035380
113169845031698451AG37GENIChomozygous115812402
113169923331699234AG39GENIChomozygous115812404
113169928931699290GA29GENIChomozygous116035382
113170063131700632TC38GENIChomozygous115812406
113170071331700714CG41GENIChomozygous115812408
113170124531701246AG29GENICpossibly homozygous115812410
113170133631701337CG30GENIChomozygous115812412
113170150931701510CT30GENIChomozygous116035384
113170157931701580AG29GENIChomozygous115812414
113170222531702226CT41GENIChomozygous116035386
113170261331702614TC41GENIChomozygous115812416
113170279731702798CT35GENIChomozygous115812418
113170291631702917TC35GENIChomozygous115812420
113170402731704028GA46GENIChomozygous116035388
113170545131705452AG41GENIChomozygous115812424
113170570531705706GA29GENIChomozygous115812426
113170572031705721CA34GENIChomozygous115812428
113170633031706331GA42GENIChomozygous115812430
113170669731706698TA31GENIChomozygous115812432
113170693031706931CT28GENIChomozygous116035390
113170720131707202TA24GENIChomozygous115960358
113170828331708284CT43GENIChomozygous115812440
113171009431710095GA49GENIChomozygous115812444
113171190031711901CT52GENICpossibly homozygous116035392
113171230131712302AG37GENICpossibly homozygous115812450
113170343831703439CT40GENIChomozygous118203030