| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33418086-33418659 | Common:3; Rare:122 | ||||
| chr6:33419137-33420031 | Common:2; Rare:185 | ||||
| chr6:33420188-33421180 | Common:5; Rare:261; Clinvar (benign):11 | ||||
| chr6:33454363-33454685 | Common:1; Rare:90 | ||||
| chr6:33580171-33580376 | Common:2; Rare:56 | ||||
| chr6:33711634-33711909 | Common:2; Rare:106; Clinvar (benign):1 | ||||
| chr6:33788285-33788429 | Rare:49 | ||||
| chr6:33789088-33789283 | Common:2; Rare:92 | ||||
| chr6:34236667-34236938 | Common:3; Rare:125 | ||||
| chr6:34248970-34249390 | Common:1; Rare:101 | ||||
| chr6:34392580-34392954 | Common:2; Rare:117 | ||||
| chr6:34425997-34426278 | Common:5; Rare:109; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696821-34697000 | Rare:42 | ||||
| chr6:34757283-34757532 | Common:2; Rare:65 | ||||
| chr6:34791937-34792119 | Common:3; Rare:55 |