chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152867598528675986CA21GENIChomozygous884565303
152867613328676134TG18GENIChomozygous884565304
152867702328677024CT9GENICheterozygous884565305
152867737828677379AT9GENIChomozygous884565306
152867780428677805CT20GENIChomozygous884565307
152867980328679804CA18GENIChomozygous884565308
152867984128679842CT20GENIChomozygous884565309
152868039528680396CG20GENIChomozygous884565310
152868042628680427GT22GENICpossibly homozygous884565311
152868059428680595GA10GENIChomozygous884565312
152868210428682105GA12GENIChomozygous884565313
152868348528683486TG17GENIChomozygous884565314
152868423428684235AG20GENIChomozygous884565315
152868560028685601TC22GENIChomozygous884565316
152868600228686003GA5GENICheterozygous884565317
152868601728686018GT8GENIChomozygous884565318
152868749228687493GA26GENIChomozygous884565319
152868767128687672AT27GENIChomozygous884565320
152868794528687946CT19GENIChomozygous884565321
152868804028688041GT8GENIChomozygous884565322
152868830328688304GA10GENIChomozygous884565323
152868867828688679CT15GENIChomozygous884565324
152868903028689031GA10GENIChomozygous884565325
152868926328689264GA8GENICheterozygous884565326
152869139828691399AG22GENIChomozygous884565327
152869156128691562AC18GENIChomozygous884565328
152869223728692238TC10GENIChomozygous884565329
152869238128692382CT14GENIChomozygous884565330
152869302128693022GA18GENIChomozygous884565331
152869343828693439AC8GENIChomozygous884565332
152869371328693714AG12GENICheterozygous884565333
152869492328694924GA11GENICheterozygous884565334
152869553928695540TC22GENIChomozygous884565335
152869559828695599GA5GENIChomozygous884565336
152869599128695992GA15GENIChomozygous884565337