chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105495827854958279AT15GENIChomozygous142248624
105495836454958365CA15GENIChomozygous142248625
105495867854958679GA16GENIChomozygous142248626
105495869554958696TC18GENIChomozygous142248627
105495884554958846GC13GENIChomozygous142248628
105495913654959137GA18GENIChomozygous142248629
105495956254959563TG16GENIChomozygous142248630
105495970954959710TG14GENIChomozygous142248631
105495974054959741TC18GENIChomozygous142248632
105495977854959779GA20GENIChomozygous142248633
105496001654960016A10GENICpossibly homozygous142203588
105496003854960039T10GENIChomozygous142203589
105496068554960686GA16GENIChomozygous142248634
105496151754961518AT19GENIChomozygous142248635
105496174454961745AG13GENIChomozygous142248636
105496221454962215GC14GENIChomozygous142248637
105496250554962506AG14GENIChomozygous142248638
105496274054962741GA16GENIChomozygous142248639
105496317054963171TC16GENIChomozygous142248640
105496349154963492AG17GENIChomozygous142248641
105496386554963866TG15GENIChomozygous142248642
105496411854964119AG14GENIChomozygous142248643
105496434454964345GA19GENIChomozygous142248644
105496500554965006AG17GENIChomozygous142248645
105496535154965352CT21GENIChomozygous142248646
105496611754966118TC19GENIChomozygous142248647
105496687454966875CT14GENIChomozygous142248648
105496879554968796TA14GENIChomozygous142248649
105496973754969738AG12GENIChomozygous142248650
105497008454970085TC13GENIChomozygous142248651
105497011554970116AG15GENIChomozygous142248652
105497012254970123CT12GENIChomozygous142248653