chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
202689336326893364CT23GENIChomozygous109154039
202690000426900005AG7GENIChomozygous109247240
202690056326900564AG13GENIChomozygous109247242
202690119826901199GA14GENIChomozygous109247244
202690170026901701TC17GENIChomozygous109247246
202690339826903399CT11GENIChomozygous109247248
202690457526904576AT26GENIChomozygous109154049
202690494626904947AG23GENIChomozygous109154051
202690580526905806TC20GENIChomozygous109247250
202690591526905916AT13GENIChomozygous109247252
202690614426906145CT21GENIChomozygous109247254
202690640126906402TA14GENIChomozygous109154053
202690653626906537GA14GENIChomozygous109247256
202690661326906614CG13GENIChomozygous109154055
202690698426906985AG10GENIChomozygous109247258
202690702226907023TC13GENICheterozygous109247260
202690722026907221CT27GENICpossibly homozygous109373022
202690732226907323GA21GENIChomozygous109154057
202690795426907955CT14GENIChomozygous109247262
202690796526907966GA14GENIChomozygous109154061
202690818726908188GT21GENIChomozygous109247264
202690836526908366CT10GENIChomozygous109247266
202690850726908508TC17GENIChomozygous109247268
202690854926908550AG20GENICpossibly homozygous109247270
202690936026909361TG16GENIChomozygous109247272
202690939626909397AC19GENIChomozygous109247274
202691031326910314GA11GENICpossibly homozygous109247276
202691036826910369CT11GENIChomozygous109154063
202691060826910609TC21GENIChomozygous109154065
202691095726910958AT18GENIChomozygous109247278
202691118326911184AG20GENIChomozygous109247280
202691144926911450CT8GENIChomozygous109247282
202691168426911685GT21GENIChomozygous109247284
202691245726912458AG17GENIChomozygous109247286
202691270926912710GA14GENIChomozygous109247288
202691120326911204AG17GENIChomozygous109310183
202690439726904398CT16GENICheterozygous119872264
202690443726904438TC7GENIChomozygous119838087
202690898526908986TC33GENICheterozygous119838088