chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103869444838694449CG27GENIChomozygous116565385
103869577638695777TC28GENIChomozygous116762346
103869855038698551GA11GENIChomozygous116762352
103870564438705645GA11GENIChomozygous116762360
103870609538706096GA16GENIChomozygous117126008
103869929938699300GA19GENIChomozygous117126002
103870439338704394CT11GENIChomozygous117126004
103870032038700321CT9GENIChomozygous116925200
103870778638707787TA10GENIChomozygous116762362
103870795238707953GA11GENIChomozygous117126010
103871621538716216CT18GENIChomozygous116925206
103871724838717249GA28GENIChomozygous117126012
103871912038719121TC6GENIChomozygous116925208
103872348338723484TA30GENIChomozygous116762382
103872578038725781GC31GENIChomozygous116762384
103873168538731686AG21GENIChomozygous117126014
103873232238732323TA12GENIChomozygous116925212
103873811238738113TC33GENIChomozygous117126016
103874207238742073AG21GENIChomozygous116869779
103874506938745070AT10GENIChomozygous116762402
103874624138746242CG28GENIChomozygous116762406
103874680438746805GT15GENIChomozygous116762408
103874721938747220AG18GENIChomozygous116762412
103875255038752551CT22GENIChomozygous116925218
103875435038754351GA14GENIChomozygous116762422
103875707638757077TG16GENIChomozygous116762424
103876007838760079CT18GENIChomozygous117126018
103876060738760608AG19GENIChomozygous116762428
103876407238764073GA25GENIChomozygous117126020
103876823338768234AG14GENIChomozygous116762440
103877230938772310CT25GENIChomozygous117126022
103877300338773004AG22GENIChomozygous116925222
103874705138747052AG32GENIChomozygous117312368