Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87818126-87818339 | Common:1; Rare:73 | ||||
chr10:88952750-88952797 | Rare:8; Clinvar:1 | ||||
chr10:88990148-88990283 | Common:2; Rare:18 | ||||
chr10:88990514-88990858 | Common:5; Rare:95; Clinvar (benign):5 | ||||
chr10:88991280-88991451 | Common:2; Rare:35 | ||||
chr10:89414664-89414778 | Common:2; Rare:55 | ||||
chr10:89701440-89701638 | Common:1; Rare:53 | ||||
chr10:92290998-92291352 | Common:5; Rare:113 | ||||
chr10:92592952-92593169 | Common:3; Rare:63 | ||||
chr10:93702493-93702682 | Common:4; Rare:67 | ||||
chr10:95693879-95694249 | Common:5; Rare:116; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:96130219-96130345 | Rare:46 | ||||
chr10:97426050-97426298 | Common:2; Rare:105 | ||||
chr10:97445981-97446225 | Rare:63 | ||||
chr10:97498382-97498560 | Common:2; Rare:69 |