chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143537295435372955TC48GENIChomozygous65908344
143537648935376490TG37GENIChomozygous65908350
143538073835380739CT34GENIChomozygous65908356
143538121335381214TC30GENIChomozygous65908358
143538223635382237GA12GENIChomozygous65908360
143538378135383782AG26GENIChomozygous65908362
143538544635385447GA37GENIChomozygous65908368
143538856135388562AG34GENIChomozygous65908370
143538874335388744TA7GENIChomozygous65908372
143539089735390898TG31GENIChomozygous65908374
143539201035392011AC24GENIChomozygous65908376
143539290335392904CT30GENICheterozygous66414175
143539420035394201AG35GENIChomozygous65908412
143539780935397810AG30GENIChomozygous65908418
143539797535397976AG28GENICpossibly homozygous65908420
143539925235399253CA12GENIChomozygous65908422
143539961135399612TA30GENIChomozygous65908424
143539968335399684GA28GENIChomozygous65908426
143539991335399914GA36GENIChomozygous65908428
143540065535400656AC22GENIChomozygous65908430
143540069235400693TC20GENIChomozygous65908432
143540097835400979GA35GENIChomozygous66283088
143540097935400980AC35GENIChomozygous65908434
143540209635402097AT30GENIChomozygous65908438
143540349635403497TA32GENIChomozygous65908440
143540409535404096GA45GENIChomozygous65908442
143540450435404505CT23GENICpossibly homozygous65908444
143540466135404662CT26GENICpossibly homozygous65908446
143540466435404665CT27GENICpossibly homozygous65908448
143540581935405820TC18GENIChomozygous65908450
143540587935405880TC23GENIChomozygous65908452
143540796235407963GA34GENIChomozygous65908458
143540855935408560GA31GENIChomozygous65908460
143540943735409438AG18GENIChomozygous65908462
143540960735409608AT33GENIChomozygous65908464
143541081335410814AG35GENIChomozygous65908466
143541176535411766CA33GENIChomozygous65908468
143541221935412220GA14GENIChomozygous65908470
143541225535412256AG7GENIChomozygous65908472
143541567135415672TG32GENIChomozygous65908474
143541697435416975TC50GENIChomozygous65908476
143541757135417572GA36GENIChomozygous65908478