chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135103451251034513TC18GENIChomozygous114342403
135103515351035154AG22GENIChomozygous114342405
135103560151035602TC19GENIChomozygous114342407
135103619951036200GT13GENICpossibly homozygous114342409
135103661651036617AG18GENIChomozygous114342411
135103681851036819TC16GENIChomozygous114342413
135103790151037902TA25GENIChomozygous114342415
135103937351039374TC20GENIChomozygous114342417
135103942251039423GA21GENIChomozygous114342419
135104023551040236GA28GENIChomozygous114342421
135104054251040543TG29GENIChomozygous114342423