chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1835654283565429TG28GENIChomozygous110518422
1835654663565467TC26GENIChomozygous110518424
1835655363565537TG25GENIChomozygous110518426
1835657873565788CG43GENIChomozygous110241951
1835662753566276CG35GENICpossibly homozygous110241953
1835663353566336CT36GENIChomozygous110241956
1835664923566493TC45GENICpossibly homozygous110518428
1835668313566832TG36GENICpossibly homozygous110241958
1835719833571984TC34GENIChomozygous110518430
1835721333572134TC31GENIChomozygous110241960
1835725063572507AG42GENIChomozygous110241962
1835747233574724CT24GENIChomozygous110518432
1835785653578566CT37GENIChomozygous110241964
1835795903579591CT34GENIChomozygous110241966
1835837023583703CT31GENIChomozygous110241970
1835853953585396GA23GENIChomozygous110241973
1835666523566652CCCCT23GENIChomozygous129506041
1835750533575053T22GENICpossibly homozygous129506042
1835826613582666TGCTA40GENIChomozygous129506043
1835783323578334CC29GENIChomozygous132225369
1835849953584995T29GENICpossibly homozygous132225370
1835854453585446T25GENIChomozygous129506044
1835854473585449CT25GENIChomozygous129506045
1835895983589599AG40GENIChomozygous110518434
1835898413589842GC24GENIChomozygous110518436
1835899113589912TC22GENIChomozygous110518439