chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143537295435372955TC14GENIChomozygous65908344
143537648935376490TG28GENIChomozygous65908350
143538073835380739CT27GENIChomozygous65908356
143538121335381214TC16GENIChomozygous65908358
143538223635382237GA8GENIChomozygous65908360
143538378135383782AG25GENIChomozygous65908362
143538544635385447GA15GENIChomozygous65908368
143538856135388562AG9GENIChomozygous65908370
143538874335388744TA22GENIChomozygous65908372
143539089735390898TG26GENIChomozygous65908374
143539201035392011AC22GENIChomozygous65908376
143539420035394201AG8GENIChomozygous65908412
143539780935397810AG33GENIChomozygous65908418
143539797535397976AG31GENIChomozygous65908420
143539925235399253CA27GENIChomozygous65908422
143539961135399612TA33GENIChomozygous65908424
143539968335399684GA20GENIChomozygous65908426
143539991335399914GA24GENIChomozygous65908428
143540065535400656AC13GENIChomozygous65908430
143540097835400979GA23GENIChomozygous66283088
143540097935400980AC22GENIChomozygous65908434
143540209635402097AT24GENIChomozygous65908438
143540349635403497TA28GENIChomozygous65908440
143540409535404096GA24GENIChomozygous65908442
143540450435404505CT10GENIChomozygous65908444
143540466135404662CT16GENIChomozygous65908446
143540466435404665CT17GENICpossibly homozygous65908448
143540581935405820TC31GENIChomozygous65908450
143540587935405880TC23GENIChomozygous65908452
143540796235407963GA6GENIChomozygous65908458
143540855935408560GA17GENIChomozygous65908460
143540943735409438AG16GENIChomozygous65908462
143540960735409608AT14GENIChomozygous65908464
143541081335410814AG26GENIChomozygous65908466
143541176535411766CA17GENIChomozygous65908468
143541221935412220GA11GENIChomozygous65908470
143541225535412256AG4GENIChomozygous65908472
143541567135415672TG20GENIChomozygous65908474
143541697435416975TC10GENIChomozygous65908476
143541757135417572GA13GENIChomozygous65908478