chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117163869171638747CCTCTGCTCGCTTCCCCCTCCGTGTGGGCCTCTGCTCGCTTCCCCCTCCGTGTGGG--------------------------------------------------------6GENIChomozygous51218442
117164422971644230AT15GENIChomozygous50822470
117164582571645826CCT6GENIChomozygous51241420
117164750171647502CT9GENICpossibly homozygous50822474
117164820771648208TC23GENIChomozygous50822476
117164865671648657AC14GENIChomozygous50822478
117164869771648698GA19GENIChomozygous50822480
117165024071650241T-1GENIChomozygous50822482
117165056171650562GA16GENIChomozygous50822484
117165061071650611GA14GENIChomozygous50822486
117165100671651007CT19GENIChomozygous50822487
117165159171651592C-5GENIChomozygous51218444
117165175571651756TC11GENIChomozygous50822489
117165247771652478TC27GENIChomozygous50822491
117165263371652634CCT28GENIChomozygous50822493
117165465071654651GT16GENIChomozygous50822494
117165480871654809TC16GENIChomozygous50822496
117165518871655189CT21GENIChomozygous50822497
117165558971655590G-10GENIChomozygous50822499
117165671071656711AG20GENIChomozygous50822500
117165719671657206ACACACACAC----------2GENIChomozygous51218446
117165775671657757TC22GENIChomozygous50822501
117165871971658720CT17GENIChomozygous50822503
117165902371659024GA20GENIChomozygous50822505
117166031471660315CT12GENIChomozygous50822514
117165907371659074TC20GENIChomozygous50822507
117165931971659320AG16GENIChomozygous50822509
117165932071659321AC17GENIChomozygous50822511
117165966571659666CT23GENIChomozygous50822513
117166076071660761TG22GENIChomozygous50822516
117166081371660814TG19GENICpossibly homozygous51218448
117166082071660822TG--18GENICpossibly homozygous51218450
117166156771661568GA15GENIChomozygous50822517
117166176371661764TG15GENIChomozygous50822519
117166323271663233AG19GENIChomozygous50822521
117166335471663355TG15GENIChomozygous50822523