chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265426401265426402CT7GENIChomozygous61194226
1265433734265433735AAGAG2GENIChomozygous62213678
1265434277265434278AC20GENIChomozygous61194232
1265434406265434407TG22GENIChomozygous61194234
1265434746265434747CCT11GENIChomozygous61194236
1265435420265435421TA33GENIChomozygous61194238
1265435693265435694TC22GENIChomozygous61194240
1265435696265435697CA22GENIChomozygous61194242
1265435923265435924GA24GENIChomozygous61194244
1265436393265436394AG25GENIChomozygous61194246
1265436394265436395TTG18GENIChomozygous61194248
1265436395265436396TTA18GENICpossibly homozygous62375419
1265436395265436396TTGTA18GENICheterozygous62635667
1265436506265436507TC23GENIChomozygous61194252
1265436564265436565AAAC8GENICpossibly homozygous61194254
1265437098265437120CTCTCTCTCTCTCTCCCTCTCT----------------------10GENICpossibly homozygous62375420
1265437194265437195AATCT21GENIChomozygous61194258
1265437709265437710TA25GENIChomozygous61194260
1265438573265438574AG7GENIChomozygous61194262
1265438982265438983GA27GENIChomozygous61194264
1265439435265439436A-15GENIChomozygous62375421
1265439437265439438TTCA17GENIChomozygous62375422
1265439877265439878T-4GENICheterozygous62280535
1265440062265440063GGC26GENICheterozygous62112064
1265440405265440406CCT15GENIChomozygous61194276
1265443585265443586CG35GENIChomozygous61194292
1265443589265443590AG33GENIChomozygous61194294
1265443691265443692AT21GENIChomozygous61194296
1265444734265444735CG48GENIChomozygous61194297
1265446045265446046TC23GENIChomozygous61194301
1265446621265446622TC16GENIChomozygous61194303
1265447184265447188CCCC----16GENIChomozygous61194305
1265448505265448506TC19GENIChomozygous61194307
1265449424265449425AG23GENIChomozygous61194309
1265450496265450497AG14GENIChomozygous61194311
1265451897265451898TC24GENIChomozygous61194312
1265453399265453400AT17GENIChomozygous61194314