chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403319614033197TC26INTERGENICpossibly homozygous68323344
101403510314035104TA17INTERGENIChomozygous68323346
101403573514035736GA21INTERGENIChomozygous68323348
101403640814036409CG22INTERGENIChomozygous68323350
101403704114037042CT16INTERGENIChomozygous68323352
101403747514037476GA18INTERGENIChomozygous68323356
101403768314037684AG35INTERGENIChomozygous68323358
101403795014037951GA27INTERGENIChomozygous68323360
101403802814038029TC35INTERGENIChomozygous68323362
101403838314038384TC29INTERGENIChomozygous68323364
101403858414038585TC22INTERGENIChomozygous68323366
101403897814038979GA28INTERGENIChomozygous68323370
101403915414039155GA22INTERGENIChomozygous68323372
101403969614039697CA24INTERGENIChomozygous68323374
101404051414040515AG22INTERGENIChomozygous68323376
101404128514041286AG23INTERGENIChomozygous68323378
101404160614041607TG13INTERGENIChomozygous68323381
101404226714042268GA25INTERGENIChomozygous68323383
101404242614042427TC21INTERGENIChomozygous68323385
101404254814042549TC31INTERGENIChomozygous68323387
101404275314042754TC34INTERGENIChomozygous68323389
101404325014043251TC19INTERGENIChomozygous68323391
101404332214043323TA22INTERGENIChomozygous68323393
101404339314043394GT23INTERGENIChomozygous68323395
101404377414043775CT17INTERGENIChomozygous68323397
101404532214045323TC31INTERGENIChomozygous69020955
101404535014045351AG30INTERGENIChomozygous68323399
101404623014046231TC26INTERGENIChomozygous68323401
101404638514046386TC19INTERGENIChomozygous68323403