chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4142732889142732890CT4GENICheterozygous57943287
4142732890142732891AG3GENICheterozygous57943290
4142733328142733329GA24GENIChomozygous57943293
4142733528142733529GT8GENICpossibly homozygous57943295
4142733596142733597AT5GENIChomozygous57943298
4142734298142734299GA12GENICheterozygous56961150
4142735752142735753C-4GENIChomozygous56961151
4142735992142735993C-10GENICpossibly homozygous57943304
4142736306142736307TC22GENIChomozygous57943310
4142737015142737016GA17GENICpossibly homozygous57943313
4142738759142738760CG14GENIChomozygous57943317
4142739313142739314C-9GENICheterozygous57504956
4142739362142739363GC13GENICpossibly homozygous57943320
4142739595142739596C-1GENIChomozygous57943323
4142740601142740602AT7GENIChomozygous57943326