chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143537295435372955TC49GENIChomozygous65908344
143537648935376490TG48GENIChomozygous65908350
143538073835380739CT52GENIChomozygous65908356
143538121335381214TC41GENIChomozygous65908358
143538223635382237GA15GENIChomozygous65908360
143538378135383782AG36GENIChomozygous65908362
143538544635385447GA39GENIChomozygous65908368
143538856135388562AG42GENIChomozygous65908370
143538874335388744TA25GENIChomozygous65908372
143539089735390898TG43GENIChomozygous65908374
143539201035392011AC49GENIChomozygous65908376
143539420035394201AG49GENIChomozygous65908412
143539780935397810AG37GENICheterozygous65908418
143539797535397976AG36GENICpossibly homozygous65908420
143539925235399253CA24GENICpossibly homozygous65908422
143539961135399612TA44GENIChomozygous65908424
143539968335399684GA60GENIChomozygous65908426
143539991335399914GA45GENIChomozygous65908428
143540065535400656AC26GENIChomozygous65908430
143540069235400693TC30GENIChomozygous65908432
143540097835400979GA54GENIChomozygous66283088
143540097935400980AC54GENIChomozygous65908434
143540209635402097AT63GENIChomozygous65908438
143540349635403497TA41GENIChomozygous65908440
143540409535404096GA67GENIChomozygous65908442
143540450435404505CT24GENIChomozygous65908444
143540466135404662CT32GENICpossibly homozygous65908446
143540466435404665CT32GENICpossibly homozygous65908448
143540581935405820TC47GENIChomozygous65908450
143540587935405880TC51GENIChomozygous65908452
143540796235407963GA23GENIChomozygous65908458
143540855935408560GA42GENIChomozygous65908460
143540943735409438AG27GENIChomozygous65908462
143540960735409608AT40GENIChomozygous65908464
143541081335410814AG65GENIChomozygous65908466
143541176535411766CA44GENIChomozygous65908468
143541221935412220GA20GENIChomozygous65908470
143541225535412256AG12GENIChomozygous65908472
143541567135415672TG41GENIChomozygous65908474
143541697435416975TC34GENIChomozygous65908476
143541757135417572GA39GENIChomozygous65908478