chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
19006600290066003AG18GENIChomozygous61461253
19006623390066234CCTGAGT13GENIChomozygous61461255
19006628790066288CG15GENIChomozygous61461257
19006672190066722AG21GENIChomozygous61461259
19006695990066960GA25GENIChomozygous61461261
19006714590067146AT16GENICpossibly homozygous61461263
19006727290067280GGTGAGCG--------16GENICpossibly homozygous61461265
19006737990067380AG8GENIChomozygous61461267
19006755790067558AG9GENIChomozygous61461275
19006756990067570AG7GENIChomozygous61461277
19006757190067572AG7GENIChomozygous61461278
19006758990067590GGTGGGTGAGCAGGTGAGAGGGTGAA10GENICheterozygous62263783
19006759590067596GGAACTGATA8GENICheterozygous62263784
19006760790067608TG8GENICheterozygous61461286
19006816690068167AG12GENIChomozygous61461305
19006796890067969CT13GENIChomozygous61461302
19006801890068019AAAGG22GENIChomozygous61461304
19006816790068168AG13GENIChomozygous61461307
19006876690068767TC22GENIChomozygous61461309
19006882090068821GA21GENIChomozygous62569571
19006886290068863AG28GENIChomozygous61461311
19006895290068953CG23GENIChomozygous61461313
19006988590069886AT21GENIChomozygous62480721
19007023090070233TTT---14GENIChomozygous61461321
19007129090071292AA--6GENICheterozygous62245453
19007129190071292A-6GENICheterozygous62311319
19007185290071853TC8GENIChomozygous61461326
19007289890072899CCTTT10GENICheterozygous61887582
19007289890072899CCTT10GENICheterozygous62140240
19007292790072928AG18GENIChomozygous61461328
19007292890072929CG18GENIChomozygous61461330
19007321290073213AG11GENIChomozygous61461331
19007409690074097AG13GENIChomozygous61461333
19007443690074437TC13GENIChomozygous61461335
19007537190075372AG9GENIChomozygous61887586