| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33299370-33299532 | Common:1; Rare:39 | ||||
| chr6:33313543-33314288 | Common:9; Rare:220; Clinvar:1 | ||||
| chr6:33319883-33320591 | Common:3; Rare:221; Clinvar (pathogenic):1 | ||||
| chr6:33322064-33322175 | Common:2; Rare:26 | ||||
| chr6:33322861-33323220 | Common:5; Rare:122 | ||||
| chr6:33411026-33411205 | Rare:32 | ||||
| chr6:33414331-33414547 | Common:2; Rare:49 | ||||
| chr6:33417803-33418474 | Common:3; Rare:190 | ||||
| chr6:33420131-33420303 | Rare:35; Clinvar (benign):1 | ||||
| chr6:33438657-33438905 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:33454378-33454610 | Rare:68 | ||||
| chr6:33784353-33784477 | Common:3; Rare:37 | ||||
| chr6:33788375-33788435 | Rare:15 | ||||
| chr6:34236752-34237064 | Common:2; Rare:126 | ||||
| chr6:34392266-34392774 | Common:1; Rare:186 |