chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113169465431694655TC42GENIChomozygous115812390
113169481331694814GT22GENIChomozygous115812392
113169570831695709AG19GENIChomozygous115812394
113169629431696295CG15GENIChomozygous115812396
113169693831696939AC22GENIChomozygous115812398
113169739331697394AG24GENIChomozygous115812400
113169845031698451AG31GENIChomozygous115812402
113169923331699234AG19GENIChomozygous115812404
113170063131700632TC43GENIChomozygous115812406
113170071331700714CG35GENIChomozygous115812408
113170124531701246AG35GENIChomozygous115812410
113170133631701337CG36GENIChomozygous115812412
113170157931701580AG32GENIChomozygous115812414
113170261331702614TC24GENIChomozygous115812416
113170279731702798CT23GENIChomozygous115812418
113170291631702917TC26GENIChomozygous115812420
113170494931704950CT31GENIChomozygous115812422
113170545131705452AG25GENIChomozygous115812424
113170633031706331GA18GENIChomozygous115812430
113170669731706698TA16GENIChomozygous115812432
113170720131707202TA20GENIChomozygous115960358
113170750231707503AC31GENIChomozygous115812434
113170751731707518CT29GENIChomozygous115812436
113170759531707596GA25GENIChomozygous115812438
113170828331708284CT29GENIChomozygous115812440
113170930531709306GT44GENIChomozygous115812442
113171009431710095GA26GENIChomozygous115812444
113171095531710956GA17GENIChomozygous115812446
113171162931711630TA25GENIChomozygous115812448
113171202231712023AG31GENIChomozygous115960359
113171208931712090GA20GENIChomozygous115960360