chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143537295435372955TC24GENIChomozygous65908344
143537648935376490TG24GENIChomozygous65908350
143538073835380739CT27GENIChomozygous65908356
143538121335381214TC17GENIChomozygous65908358
143538223635382237GA10GENIChomozygous65908360
143538378135383782AG23GENIChomozygous65908362
143538544635385447GA20GENIChomozygous65908368
143538856135388562AG19GENIChomozygous65908370
143538874335388744TA11GENIChomozygous65908372
143539089735390898TG24GENIChomozygous65908374
143539201035392011AC18GENIChomozygous65908376
143539420035394201AG11GENIChomozygous65908412
143539780935397810AG59GENIChomozygous65908418
143539797535397976AG47GENIChomozygous65908420
143539925235399253CA21GENIChomozygous65908422
143539961135399612TA27GENIChomozygous65908424
143539968335399684GA43GENIChomozygous65908426
143539991335399914GA23GENIChomozygous65908428
143540065535400656AC18GENIChomozygous65908430
143540069235400693TC22GENICpossibly homozygous65908432
143540097835400979GA18GENIChomozygous66283088
143540097935400980AC17GENIChomozygous65908434
143540209635402097AT19GENIChomozygous65908438
143540349635403497TA31GENIChomozygous65908440
143540409535404096GA21GENIChomozygous65908442
143540450435404505CT11GENICheterozygous65908444
143540466135404662CT17GENIChomozygous65908446
143540466435404665CT17GENIChomozygous65908448
143540581935405820TC22GENIChomozygous65908450
143540587935405880TC27GENIChomozygous65908452
143540796235407963GA18GENIChomozygous65908458
143540855935408560GA21GENIChomozygous65908460
143540943735409438AG25GENIChomozygous65908462
143540960735409608AT26GENIChomozygous65908464
143541081335410814AG29GENIChomozygous65908466
143541176535411766CA20GENIChomozygous65908468
143541221935412220GA8GENIChomozygous65908470
143541225535412256AG4GENIChomozygous65908472
143541567135415672TG15GENIChomozygous65908474
143541697435416975TC10GENIChomozygous65908476
143541757135417572GA16GENIChomozygous65908478