chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
202689336326893364CT22GENIChomozygous109154039
202690000426900005AG8GENIChomozygous109247240
202690056326900564AG13GENIChomozygous109247242
202690119826901199GA14GENIChomozygous109247244
202690339826903399CT11GENIChomozygous109247248
202690416926904170TC23GENICpossibly homozygous109310181
202690494626904947AG22GENIChomozygous109154051
202690580526905806TC20GENIChomozygous109247250
202690614426906145CT19GENIChomozygous109247254
202690640126906402TA14GENIChomozygous109154053
202690653626906537GA12GENIChomozygous109247256
202690661326906614CG13GENIChomozygous109154055
202690732226907323GA20GENIChomozygous109154057
202690795426907955CT12GENIChomozygous109247262
202690796526907966GA13GENIChomozygous109154061
202690818726908188GT20GENIChomozygous109247264
202690836526908366CT10GENIChomozygous109247266
202690850726908508TC18GENIChomozygous109247268
202690854926908550AG20GENIChomozygous109247270
202690939626909397AC17GENIChomozygous109247274
202691031326910314GA8GENICpossibly homozygous109247276
202691036826910369CT10GENIChomozygous109154063
202691060826910609TC20GENIChomozygous109154065
202691095726910958AT21GENIChomozygous109247278
202691118326911184AG17GENIChomozygous109247280
202691120326911204AG17GENIChomozygous109310183
202691144926911450CT9GENIChomozygous109247282
202691168426911685GT22GENIChomozygous109247284
202691245726912458AG17GENIChomozygous109247286
202691270926912710GA14GENIChomozygous109247288