chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101355354113553541G16GENICheterozygous128790627
101355361313553614GA41GENIChomozygous118030369
101355528113555282TC67GENIChomozygous116496234
101355568213555683TC76GENIChomozygous116496236
101355571113555712AG72GENIChomozygous116496238
101355622313556224CT63GENIChomozygous117249121
101355923113559232A57GENIChomozygous128790629
101355993813559939CT54GENIChomozygous117249123
101356032013560321AG53GENIChomozygous116496246
101356143613561437AG53GENIChomozygous116735865
101356413513564136AG23GENIChomozygous116496256
101356471313564714CT57GENIChomozygous117249125
101356563213565633AG57GENIChomozygous118030371
101356586213565863GA52GENIChomozygous116496258
101356645513566456AC54GENIChomozygous116496264
101356800113568002CT65GENICpossibly homozygous117249127
101356938413569385GA57GENIChomozygous117249129
101356982613569827CT70GENIChomozygous117249131
101356220413562204G49GENIChomozygous131463466
101357292113572922CT52GENIChomozygous117249133
101357370413573706GG45GENIChomozygous131463467
101357370713573709AG45GENIChomozygous131463468
101357410113574102TC59GENIChomozygous116496282
101357568713575688AT43GENIChomozygous117249135