chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157127932157127933CT48GENIChomozygous112905477
4157128941157128942TG63GENIChomozygous112905479
4157129150157129151AG58GENIChomozygous112905481
4157129153157129154GC55GENIChomozygous112905483
4157129293157129294TG64GENICpossibly homozygous112905485
4157130255157130256AG79GENIChomozygous112905487
4157130261157130261TATAGGTCTAGAATAGCTCCCC77GENIChomozygous128096027
4157130302157130303GA62GENIChomozygous112905489
4157130649157130650CG64GENIChomozygous112905491
4157131094157131095TA53GENIChomozygous112905493
4157131510157131510GAA23GENIChomozygous128096028
4157132353157132354AG50GENIChomozygous112905495
4157132776157132777TG49GENIChomozygous112905497
4157133713157133714CT37GENIChomozygous112905499
4157133758157133759CT36GENIChomozygous112905501
4157134281157134282TA53GENIChomozygous112905507
4157134353157134354TC54GENIChomozygous112905509
4157134471157134472AT44GENIChomozygous112905511
4157134715157134716GA69GENIChomozygous112905513