chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2239017509239017510CT8GENIChomozygous110328780
2239021996239021997CT12GENIChomozygous110841568
2239022253239022254CA27GENIChomozygous110841569
2239022932239022933AC22GENIChomozygous110841570
2239029058239029059AC20GENIChomozygous110841572
2239033154239033155GA15GENIChomozygous110841573
2239037794239037795AG5GENICheterozygous120300299
2239039657239039658GA13GENIChomozygous110841575
2239040607239040608GA24GENIChomozygous110328958
2239042697239042698TA19GENIChomozygous110328960
2239043474239043475GC9GENIChomozygous110841578
2239043481239043482CG5GENIChomozygous110328964
2239043512239043513CT5GENIChomozygous110328966
2239043533239043534GA12GENIChomozygous110328968
2239043578239043579TG14GENIChomozygous110328970
2239048696239048697AT6GENIChomozygous110841582
2239048914239048915TC9GENICheterozygous125673721
2239048915239048916AC9GENICheterozygous125673723
2239051075239051076GA16GENIChomozygous110841585
2239051885239051886GA9GENIChomozygous110841586
2239054072239054073TC18GENIChomozygous110329063
2239054299239054300AG10GENIChomozygous110329065
2239055337239055338AG6GENIChomozygous110329069
2239056286239056287GA16GENIChomozygous110841587
2239056380239056381CT17GENICpossibly homozygous110329077
2239057094239057095TG9GENIChomozygous110329079
2239058148239058149AG13GENIChomozygous110329081
2239058310239058311TC17GENIChomozygous110329083
2239059225239059226AG21GENIChomozygous110329085
2239061033239061034GC9GENICheterozygous125609627
2239062103239062104AG14GENIChomozygous110329093
2239062276239062277AG13GENIChomozygous110841588
2239062822239062823TC16GENIChomozygous110329095
2239065171239065172CT10GENIChomozygous110329101
2239066532239066533TC18GENIChomozygous110329103