chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109000625190006252GA51GENIChomozygous51735633
109000633290006333T-41GENIChomozygous51735635
109000635790006358G-33GENIChomozygous51537432
109000690990006911TT--3GENIChomozygous51537436
109000708290007083T-1GENIChomozygous51735637
109000709890007099TTTC29GENICheterozygous51537438
109000748090007481C-48GENIChomozygous51537441
109000817990008180G-18GENICheterozygous51537443
109000817990008180GGT18GENICheterozygous51537444
109000895890008959CT77GENIChomozygous51735639
109000932390009324TC61GENICpossibly homozygous51537446
109000972190009722GA54GENIChomozygous51537447
109001068990010690CT67GENIChomozygous51735641