chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176416778176416779AC26GENIChomozygous882791869
3176417058176417059CT17GENIChomozygous882791870
3176417847176417848TA29GENIChomozygous882791871
3176417978176417979GA28GENIChomozygous882791872
3176420655176420656AT16GENIChomozygous882791873
3176421058176421059CT31GENIChomozygous882791874
3176423063176423064TC12GENIChomozygous882791875
3176423384176423385GA17GENIChomozygous882791876
3176423703176423704AG14GENICheterozygous882791877
3176424176176424177GA24GENIChomozygous882791878
3176426813176426814AG21GENIChomozygous882791879
3176430050176430051AC16GENIChomozygous882791880
3176430869176430870CA16GENIChomozygous882791881