| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33417855-33418498 | Common:6; Rare:353 | ||||
| chr6:33454383-33454618 | Rare:133 | ||||
| chr6:33711600-33711817 | Common:1; Rare:108; Clinvar (benign):3 | ||||
| chr6:33788062-33788462 | Common:5; Rare:202 | ||||
| chr6:33789074-33789249 | Common:2; Rare:165; Clinvar (pathogenic):1 | ||||
| chr6:34236645-34236964 | Common:6; Rare:223 | ||||
| chr6:34237296-34237669 | Common:4; Rare:185 | ||||
| chr6:34237964-34238470 | Common:10; Rare:242 | ||||
| chr6:34248981-34249325 | Common:2; Rare:147 | ||||
| chr6:34392315-34392463 | Rare:117 | ||||
| chr6:34392571-34392887 | Common:1; Rare:104 | ||||
| chr6:34425965-34426212 | Common:9; Rare:180; Clinvar:2; Clinvar (benign):16 | ||||
| chr6:34696664-34697010 | Common:2; Rare:144 | ||||
| chr6:34757309-34757596 | Common:2; Rare:160 | ||||
| chr6:34791688-34792204 | Common:11; Rare:206 |