Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:86971187-86971396 | Rare:66 | ||||
chr10:87342313-87342926 | Common:5; Rare:188 | ||||
chr10:87862236-87862598 | Rare:174; Clinvar:1 | ||||
chr10:87957746-87957978 | Rare:49; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):7 | ||||
chr10:88064910-88065224 | Common:3; Rare:58 | ||||
chr10:88104344-88104525 | Rare:25 | ||||
chr10:88108255-88108479 | Common:1; Rare:41 | ||||
chr10:88759893-88760071 | Common:2; Rare:25 | ||||
chr10:88937520-88937523 | |||||
chr10:88939505-88939900 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr10:88941760-88942136 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr10:88948800-88949117 | Rare:61; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr10:88951679-88951838 | Rare:31 | ||||
chr10:88951875-88951941 | Rare:7 | ||||
chr10:91807506-91807691 | Rare:37 |