chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1103975851103975852TG25INTERGENIChomozygous74275916
1103976823103976824GA18INTERGENICpossibly homozygous75105139
1103979736103979737TC30GENIChomozygous75105140
1103979864103979865GC25GENIChomozygous75105141
1103979872103979873TC28GENIChomozygous74275922
1103980426103980427AG25GENIChomozygous74275925
1103980564103980565TC26GENIChomozygous75105142
1103980691103980692AT19GENIChomozygous75105143
1103980743103980744CA15GENIChomozygous75105144
1103980870103980871TC34GENIChomozygous75105145
1103981130103981131CT29GENIChomozygous75105146
1103981649103981650AT24INTERGENIChomozygous75105147
1103982243103982244TC20INTERGENIChomozygous75105148
1103982637103982638CG18INTERGENIChomozygous75105149
1103982673103982674TC16INTERGENIChomozygous75105150
1103982870103982871TC14INTERGENIChomozygous75105151
1103983000103983001CG29INTERGENIChomozygous75105152
1103983071103983072CG25INTERGENIChomozygous75105153
1103983224103983225CA23INTERGENIChomozygous75105154
1103983479103983480TC21INTERGENIChomozygous75105155
1103983480103983481TC21INTERGENIChomozygous75105156
1103983559103983560GA15INTERGENIChomozygous75105157
1103983640103983641CT15INTERGENIChomozygous75105158
1103984473103984474AG16INTERGENIChomozygous75105159
1103984621103984622AC20INTERGENIChomozygous75105160