chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
202689336326893364CT18GENIChomozygous109154039
202690000426900005AG17GENIChomozygous109247240
202690056326900564AG25GENIChomozygous109247242
202690119826901199GA20GENIChomozygous109247244
202690339826903399CT19GENIChomozygous109247248
202690416926904170TC17GENIChomozygous109310181
202690494626904947AG16GENIChomozygous109154051
202690580526905806TC21GENIChomozygous109247250
202690591526905916AT21GENIChomozygous109247252
202690614426906145CT28GENIChomozygous109247254
202690640126906402TA29GENIChomozygous109154053
202690653626906537GA30GENIChomozygous109247256
202690661326906614CG33GENIChomozygous109154055
202690698426906985AG10GENIChomozygous109247258
202690702226907023TC5GENIChomozygous109247260
202690732226907323GA24GENIChomozygous109154057
202690795426907955CT18GENIChomozygous109247262
202690796526907966GA15GENIChomozygous109154061
202690818726908188GT23GENIChomozygous109247264
202690850726908508TC23GENIChomozygous109247268
202690854926908550AG27GENIChomozygous109247270
202690936026909361TG19GENIChomozygous109247272
202690939626909397AC26GENIChomozygous109247274
202691031326910314GA24GENIChomozygous109247276
202691036826910369CT29GENIChomozygous109154063
202691060826910609TC26GENIChomozygous109154065
202691095726910958AT27GENIChomozygous109247278
202691137526911376CT8GENICheterozygous109493639
202691137626911377CT10GENICheterozygous109493641
202691144926911450CT16GENIChomozygous109247282
202691168426911685GT25GENIChomozygous109247284
202691245726912458AG21GENIChomozygous109247286
202691270926912710GA30GENIChomozygous109247288