chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X123774999123775000A-14INTERGENICpossibly homozygous45214841
X123775240123775241TTG3INTERGENICheterozygous45214842
X123775380123775381CCA8INTERGENICpossibly homozygous45214843
X123775393123775394AAC6INTERGENIChomozygous45214844
X123776864123776865AG25INTERGENIChomozygous45214845
X123776908123776909CA19INTERGENIChomozygous45214846
X123777407123777408TC24INTERGENIChomozygous45214847
X123777639123777640AG18INTERGENIChomozygous45214848
X123777686123777687AG10INTERGENIChomozygous45214849
X123777689123777690GC9INTERGENICpossibly homozygous45214850
X123780357123780379GCGCGCGCGCGCGCGCGCGCGT----------------------14INTERGENICheterozygous45214851
X123781489123781490CT24INTERGENIChomozygous45214852
X123781584123781585GGAAAAAAA16INTERGENICpossibly homozygous45214853
X123781586123781588AG--16INTERGENICheterozygous45214854
X123781587123781588GGA12INTERGENICpossibly homozygous45214855
X123781865123781872GGGGGGG-------6INTERGENIChomozygous45214856
X123781881123781882GGAAAA6INTERGENIChomozygous45214857
X123781923123781924TTA12INTERGENIChomozygous45214858
X123782046123782051TTTGG-----12INTERGENIChomozygous45214859
X123783607123783611TGTG----10INTERGENIChomozygous45214860
X123784329123784330GA12INTERGENIChomozygous45214861
X123785180123785181CT23INTERGENIChomozygous45214862
X123787029123787030TC38INTERGENIChomozygous45214863