chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140271832140271833CG10INTERGENICpossibly homozygous54153298
7140273278140273279CG20INTERGENIChomozygous54153300
7140273791140273795GTGT----9INTERGENICheterozygous54153302
7140273793140273795GT--9INTERGENICheterozygous54153304
7140275490140275491TA19INTERGENICheterozygous54153308
7140276835140276836AG6INTERGENICheterozygous54153312
7140276984140276985AG1INTERGENIChomozygous54153314
7140277468140277469AG8INTERGENIChomozygous54153316
7140277611140277612TC13INTERGENIChomozygous54153318
7140277645140277646TTA18INTERGENIChomozygous54153320
7140278183140278184AG14INTERGENICpossibly homozygous54153322
7140278705140278713TTTTGTTG--------3INTERGENIChomozygous54153325
7140278877140278878CT7INTERGENICpossibly homozygous54153331
7140279461140279462TTCCCCTC1INTERGENIChomozygous55315030
7140279743140279744TC8INTERGENIChomozygous54153343
7140281093140281101GTGTGTGT--------4INTERGENICheterozygous54153345
7140282270140282271G-2INTERGENIChomozygous54153349
7140283213140283214GGTCTTT3INTERGENIChomozygous54153358
7140283320140283321CT21INTERGENICpossibly homozygous54153360
7140283726140283727AAG2INTERGENICheterozygous55315033
7140283845140283847GG--3INTERGENICheterozygous54153364
7140290449140290450AG7INTERGENICpossibly homozygous54153378
7140291159140291160TC10INTERGENIChomozygous54153380
7140291219140291220TTG3INTERGENIChomozygous54153382