chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4142732889142732890CT36GENIChomozygous57943287
4142732890142732891AG36GENIChomozygous57943290
4142733328142733329GA44GENIChomozygous57943293
4142733528142733529GT46GENIChomozygous57943295
4142733596142733597AT83GENIChomozygous57943298
4142734298142734299GA95GENICpossibly homozygous56961150
4142735752142735753C-19GENIChomozygous56961151
4142735992142735993C-13GENIChomozygous57943304
4142736306142736307TC34GENIChomozygous57943310
4142737015142737016GA55GENIChomozygous57943313
4142738759142738760CG38GENIChomozygous57943317
4142739313142739314C-16GENIChomozygous57504956
4142739362142739363GC30GENIChomozygous57943320
4142739595142739596C-38GENICpossibly homozygous57943323
4142739779142739780CCG35GENIChomozygous56961154
4142740601142740602AT56GENIChomozygous57943326
4142739629142739630GGCCCCTCC33GENIChomozygous58342131
4142735071142735084AAAAAAAAAAAAA-------------14GENIChomozygous58467335
4142737676142737677CCTTTTT6GENICheterozygous58342127
4142739622142739629GGGGGGG-------38GENIChomozygous58342129