chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3129708044129708045AAT2GENIChomozygous57670662
3129708285129708286AAG12GENIChomozygous57670664
3129708608129708609GT23GENIChomozygous57670666
3129708637129708638AG23GENIChomozygous57670668
3129708791129708792AT33GENIChomozygous57670670
3129708793129708794AAGCTGTC34GENIChomozygous57670672
3129708795129708796GC35GENIChomozygous57670674
3129709753129709754CCGTGTGTGTGT3GENICheterozygous57670676
3129709753129709754CCGTGTGTGTGTGT3GENICheterozygous58809125
3129709807129709808TC23GENIChomozygous57670678
3129710892129710893CT22GENIChomozygous57670682
3129711221129711222GA25GENIChomozygous57670684
3129711437129711438CT24GENIChomozygous57670686
3129711716129711717TA11GENIChomozygous57670688
3129711886129711887TTCACA2GENIChomozygous58695713
3129712146129712147TG13GENIChomozygous57670692
3129712681129712682CCATGCCT24GENIChomozygous57670694
3129712774129712775CT6GENIChomozygous57670696
3129713653129713654AT17GENIChomozygous57670699
3129714047129714048AG24GENIChomozygous57670701
3129714069129714072CTT---22GENIChomozygous57670703
3129714073129714076TAT---23GENIChomozygous57670705
3129714078129714079A-23GENIChomozygous57670707
3129714079129714080TG22GENIChomozygous58695714
3129715054129715055GA11GENIChomozygous57670709
3129715229129715230CCA2GENIChomozygous57670711
3129715270129715271AG12GENIChomozygous57670713
3129715333129715334TTAG13GENIChomozygous57670715
3129715518129715519CT13GENIChomozygous57670717
3129715599129715600GA16GENIChomozygous57670719
3129716465129716466CCCTGCCT13GENIChomozygous57670721
3129716495129716497TT--19GENICpossibly homozygous58695715
3129717971129717985TCAAACATGGTGTG--------------16GENIChomozygous57670723
3129717987129717994GGGGCCC-------11GENIChomozygous57670725