chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8111676152111676153TC38GENIChomozygous929627821
8111676535111676536TC41GENIChomozygous929627822
8111676727111676728AC38GENIChomozygous929627823
8111677564111677565TC42GENIChomozygous929627824
8111677792111677793AG50GENIChomozygous929627825
8111678092111678093CT36GENIChomozygous929627826
8111678149111678150AG22GENIChomozygous929627827
8111678156111678157GC19GENIChomozygous929627828
8111679047111679048CG44GENIChomozygous929627829
8111680019111680020TC47GENIChomozygous929627830
8111680058111680059TC49GENICpossibly homozygous929627831
8111682019111682020AG53GENIChomozygous929627832
8111682438111682439AG35GENIChomozygous929627833
8111683450111683451TC37GENIChomozygous929627834
8111684688111684689AG13GENIChomozygous929627835
8111684944111684945GA19GENIChomozygous929627836
8111685486111685487CT19GENIChomozygous929627837
8111685985111685986AG49GENIChomozygous929627838