chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4108140134108140135AG8GENIChomozygous113552951
4108462671108462672GT13GENIChomozygous112806658
4108493149108493150GT21GENIChomozygous112806666
4108518481108518482GT43GENIChomozygous112806676
4108544935108544936GT13GENIChomozygous112806684
4108594461108594462CA25GENIChomozygous112806688
4108544929108544930AT13GENIChomozygous119279742
4108544930108544931TA13GENIChomozygous119279744
4108629039108629040AT49GENICheterozygous113290370
4108697269108697270CA59GENIChomozygous112806720
4108824757108824758GT48GENIChomozygous112806742
4108927619108927620GC9GENIChomozygous112806766
4108980925108980926TC44GENICpossibly homozygous112806772
4109041447109041448TA31GENIChomozygous112806774