chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76116629861166299GC29GENIChomozygous785714202
76116635161166352TG28GENIChomozygous785714203
76116690261166903TC27GENIChomozygous785714204
76116842961168430TC22GENIChomozygous785714205
76116913561169136TC14GENIChomozygous785714206
76117031761170318TG18GENIChomozygous785714207
76117037961170380AT25GENIChomozygous785714208
76117107561171076GA25GENIChomozygous785714209
76117153261171533TC17GENIChomozygous785714210
76117208161172082CT38GENIChomozygous785714211
76117262561172626TA32GENIChomozygous785714212
76117326661173267GA19GENIChomozygous785714213
76118641861186419CT28GENIChomozygous785714214
76118761061187611CT26GENIChomozygous785714215
76119347861193479GA11GENICheterozygous785714216
76119355861193559GA25GENICheterozygous785714217
76119417861194179AG20GENIChomozygous785714218
76119431361194314AG10GENIChomozygous785714219
76119437761194378TG20GENIChomozygous785714220
76119797861197979TC25GENIChomozygous785714221
76119843361198434CG16GENIChomozygous785714222
76119860161198602TA22GENIChomozygous785714223
76119869661198697GA27GENIChomozygous785714224