chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143537295435372955TC23GENIChomozygous65908344
143537648935376490TG35GENIChomozygous65908350
143538073835380739CT23GENIChomozygous65908356
143538121335381214TC27GENIChomozygous65908358
143538223635382237GA9GENIChomozygous65908360
143538378135383782AG37GENIChomozygous65908362
143538544635385447GA23GENIChomozygous65908368
143538856135388562AG15GENIChomozygous65908370
143538874335388744TA25GENIChomozygous65908372
143539089735390898TG9GENIChomozygous65908374
143539201035392011AC28GENIChomozygous65908376
143539297835392979TC5GENIChomozygous66414177
143539420035394201AG14GENIChomozygous65908412
143539780935397810AG38GENIChomozygous65908418
143539797535397976AG37GENIChomozygous65908420
143539925235399253CA26GENIChomozygous65908422
143539961135399612TA28GENIChomozygous65908424
143539968335399684GA28GENIChomozygous65908426
143539991335399914GA22GENIChomozygous65908428
143540065535400656AC17GENIChomozygous65908430
143540069235400693TC19GENIChomozygous65908432
143540097835400979GA28GENIChomozygous66283088
143540097935400980AC28GENIChomozygous65908434
143540209635402097AT18GENIChomozygous65908438
143540349635403497TA29GENIChomozygous65908440
143540409535404096GA33GENIChomozygous65908442
143540450435404505CT17GENICpossibly homozygous65908444
143540466135404662CT18GENIChomozygous65908446
143540466435404665CT18GENIChomozygous65908448
143540581935405820TC21GENIChomozygous65908450
143540587935405880TC22GENIChomozygous65908452
143540796235407963GA20GENIChomozygous65908458
143540855935408560GA21GENIChomozygous65908460
143540943735409438AG23GENIChomozygous65908462
143540960735409608AT19GENIChomozygous65908464
143541081335410814AG17GENIChomozygous65908466
143541176535411766CA21GENIChomozygous65908468
143541221935412220GA9GENIChomozygous65908470
143541225535412256AG2GENIChomozygous65908472
143541567135415672TG12GENIChomozygous65908474
143541697435416975TC21GENIChomozygous65908476
143541757135417572GA13GENIChomozygous65908478