chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1103975851103975852TG32INTERGENIChomozygous74275916
1103976823103976824GA41INTERGENICpossibly homozygous75105139
1103977350103977351CT29INTERGENICheterozygous75334797
1103977352103977353AT32INTERGENICheterozygous75334798
1103977355103977356CT32INTERGENICheterozygous75334799
1103977362103977363TC28INTERGENICheterozygous75334800
1103977368103977369CT30INTERGENICheterozygous75334801
1103977409103977410TC25INTERGENICheterozygous75334802
1103977410103977411GA26INTERGENICheterozygous75334803
1103979736103979737TC36GENIChomozygous75105140
1103979864103979865GC31GENIChomozygous75105141
1103979872103979873TC34GENIChomozygous74275922
1103980426103980427AG50GENIChomozygous74275925
1103980564103980565TC29GENIChomozygous75105142
1103980691103980692AT21GENIChomozygous75105143
1103980743103980744CA29GENIChomozygous75105144
1103980870103980871TC48GENIChomozygous75105145
1103981130103981131CT49GENIChomozygous75105146
1103981649103981650AT24INTERGENIChomozygous75105147
1103982243103982244TC28INTERGENIChomozygous75105148
1103982637103982638CG18INTERGENIChomozygous75105149
1103982673103982674TC16INTERGENIChomozygous75105150
1103982870103982871TC19INTERGENIChomozygous75105151
1103983000103983001CG32INTERGENIChomozygous75105152
1103983071103983072CG30INTERGENIChomozygous75105153
1103983224103983225CA23INTERGENIChomozygous75105154
1103983479103983480TC32INTERGENIChomozygous75105155
1103983480103983481TC32INTERGENIChomozygous75105156
1103983559103983560GA18INTERGENIChomozygous75105157
1103983640103983641CT16INTERGENIChomozygous75105158
1103984473103984474AG23INTERGENIChomozygous75105159
1103984621103984622AC29INTERGENIChomozygous75105160