chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103469304034693041AC74GENIChomozygous138763713
103469316834693169AG64GENIChomozygous138763714
103469339534693395A68GENIChomozygous138678222
103469350534693506TC44GENIChomozygous138763715
103469351634693517GA43GENIChomozygous138763716
103469353434693535CA48GENIChomozygous138763717
103469401234694013CA77GENICpossibly homozygous138763718
103469403834694039CG60GENIChomozygous138763719
103469434834694349TA48GENIChomozygous138763721
103469436834694369GA46GENIChomozygous138763722
103469439934694400TA43GENIChomozygous138763723
103469444434694445CT33GENIChomozygous138763724
103469457234694573TC55GENIChomozygous138763725
103469478534694786C59GENIChomozygous138678223
103469517034695171AC53GENIChomozygous138763727
103469535934695359TTTAGTC40GENIChomozygous138678224
103469542234695423TC36GENIChomozygous138763728
103469608034696081CA80GENIChomozygous138763729
103469635334696354GA73GENIChomozygous138763730
103469707134697072AG70GENIChomozygous138763731
103469712434697125GA66GENIChomozygous138763732
103469723034697230T62GENIChomozygous138678225
103469772634697726A57GENIChomozygous138678226
103469928734699288CT58GENIChomozygous138763733
103469943834699438ATCA48GENIChomozygous138678227
103469953634699537AC67GENICpossibly homozygous138763734
103469962134699624TTA66GENIChomozygous138678229
103469962634699627A66GENIChomozygous138678230
103469986834699869TC59GENIChomozygous138763735
103469989934699900AG61GENIChomozygous138763736
103470053834700539CT58GENIChomozygous138763737
103470054834700549CT59GENIChomozygous138763738
103470058534700586TC60GENIChomozygous138763739
103470067934700680CA65GENIChomozygous138763740
103470166134701661TT65GENIChomozygous138678231
103470167734701677T70GENIChomozygous138678232
103470198934701990AG65GENIChomozygous138763742
103469984134699845CAAA62GENIChomozygous142199705
103469984634699846GTTT62GENIChomozygous142199706