chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76116629861166299GC31GENIChomozygous941353051
76116635161166352TG34GENIChomozygous941353052
76116690261166903TC20GENIChomozygous941353053
76116842961168430TC17GENIChomozygous941353054
76116913561169136TC26GENIChomozygous941353055
76116995761169958CA28GENIChomozygous941353056
76117031761170318TG26GENIChomozygous941353057
76117037961170380AT27GENIChomozygous941353058
76117107561171076GA23GENIChomozygous941353059
76117153261171533TC17GENIChomozygous941353060
76117208161172082CT13GENIChomozygous941353061
76117262561172626TA24GENIChomozygous941353062
76117326661173267GA24GENIChomozygous941353063
76118641861186419CT29GENIChomozygous941353064
76118761061187611CT24GENIChomozygous941353065
76119458461194585AG19GENIChomozygous941353066
76119797861197979TC29GENIChomozygous941353067
76119843361198434CG34GENIChomozygous941353068
76119860161198602TA22GENIChomozygous941353069
76119869661198697GA12GENIChomozygous941353070