chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135103451251034513TC12GENIChomozygous114342403
135103515351035154AG9GENIChomozygous114342405
135103560151035602TC19GENIChomozygous114342407
135103619951036200GT12GENIChomozygous114342409
135103661651036617AG16GENIChomozygous114342411
135103681851036819TC18GENICpossibly homozygous114342413
135103790151037902TA26GENIChomozygous114342415
135103937351039374TC14GENIChomozygous114342417
135103942251039423GA27GENIChomozygous114342419
135104023551040236GA17GENIChomozygous114342421
135104054251040543TG13GENIChomozygous114342423