chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108828061388280614AG21GENIChomozygous116818775
108828076988280770GA24GENIChomozygous116818777
108828212988282130GA24GENIChomozygous116818779
108828232788282328TC31GENIChomozygous116673512
108828241988282420AG31GENIChomozygous116673514
108828335688283357TC25GENIChomozygous116673520
108828391088283911AC36GENIChomozygous116818781
108828469388284694AG8GENIChomozygous116818783
108828475088284751TC16GENIChomozygous116673530
108828482188284822GA22GENIChomozygous116818785
108828502988285030CT21GENIChomozygous116818787
108828549788285498GA8GENIChomozygous116818789
108828651088286511CG34GENIChomozygous116818791
108828725088287251TC14GENIChomozygous116673532
108828726488287265AG15GENIChomozygous116901215
108828770388287704CT24GENIChomozygous117020327
108828781888287819AG14GENIChomozygous116818795
108828850388288504CA34GENIChomozygous116818797
108828854388288544TC28GENIChomozygous116673536
108828880688288807CT20GENIChomozygous116818799
108828897388288974TC21GENIChomozygous116673538
108828946588289466GA18GENIChomozygous116818801
108828968788289688AG12GENIChomozygous116673540
108829068688290687GA13GENIChomozygous116818805
108829071188290712AG16GENIChomozygous116818807
108829269688292697CA7GENICpossibly homozygous117173696
108829933888299339AG27GENIChomozygous116673558
108830247388302474TC25GENIChomozygous116673572