chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145427674145427675AT37GENIChomozygous112870872
4145428190145428191CG32GENIChomozygous112870873
4145429036145429037TC52GENIChomozygous112870874
4145429250145429251GA33GENIChomozygous112870875
4145430603145430604GC3GENIChomozygous112870877
4145431020145431021GA30GENIChomozygous112870878
4145431275145431276CT39GENIChomozygous112870879
4145431804145431805CG34GENIChomozygous112870880
4145433054145433055CT38GENIChomozygous112870881
4145433287145433288CT38GENIChomozygous112870882
4145433546145433547TC30GENIChomozygous112870883
4145433597145433598AT27GENIChomozygous112870884
4145433670145433671CT31GENIChomozygous112870885
4145434927145434928TC46GENIChomozygous112870886
4145435310145435311TC31GENIChomozygous112870887
4145435710145435711AG38GENIChomozygous112870888
4145436388145436389GC46GENIChomozygous112870889