chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113169481331694814GT10GENIChomozygous115812392
113169570831695709AG10GENIChomozygous115812394
113169629431696295CG21GENIChomozygous115812396
113169633031696331TC17GENIChomozygous116035374
113169675731696758AG23GENIChomozygous116035376
113169722031697221CT8GENIChomozygous116035378
113169739331697394AG17GENIChomozygous115812400
113169776731697768AT22GENIChomozygous116035380
113169845031698451AG17GENIChomozygous115812402
113169928931699290GA13GENIChomozygous116035382
113170063131700632TC10GENIChomozygous115812406
113170071331700714CG8GENIChomozygous115812408
113170124531701246AG20GENIChomozygous115812410
113170133631701337CG8GENIChomozygous115812412
113170150931701510CT17GENIChomozygous116035384
113170157931701580AG9GENIChomozygous115812414
113170222531702226CT13GENIChomozygous116035386
113170261331702614TC15GENIChomozygous115812416
113170279731702798CT20GENIChomozygous115812418
113170291631702917TC14GENIChomozygous115812420
113170402731704028GA15GENIChomozygous116035388
113170545131705452AG20GENIChomozygous115812424
113170570531705706GA6GENIChomozygous115812426
113170572031705721CA9GENIChomozygous115812428
113170633031706331GA20GENIChomozygous115812430
113170669731706698TA18GENIChomozygous115812432
113170693031706931CT17GENIChomozygous116035390
113170720131707202TA16GENICheterozygous115960358
113170828331708284CT18GENIChomozygous115812440
113171009431710095GA15GENIChomozygous115812444
113171190031711901CT17GENICheterozygous116035392
113171230131712302AG5GENIChomozygous115812450
113169757331697574GA5GENIChomozygous126295347