| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41740459-41740847 | Common:2; Rare:92 | ||||
| chr6:41741459-41741894 | Common:2; Rare:97 | ||||
| chr6:41742147-41742538 | Common:3; Rare:133 | ||||
| chr6:41743002-41743416 | Rare:97 | ||||
| chr6:41746582-41746679 | Common:1; Rare:8 | ||||
| chr6:41995058-41995269 | Common:2; Rare:28 | ||||
| chr6:42031235-42031370 | Common:1; Rare:22 | ||||
| chr6:42099873-42099885 | Rare:4 | ||||
| chr6:42454564-42454832 | Common:4; Rare:54 | ||||
| chr6:42783866-42783946 | Rare:17 | ||||
| chr6:42937437-42937747 | Common:2; Rare:60 | ||||
| chr6:43010614-43010902 | Rare:78 | ||||
| chr6:43042899-43043191 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:43071287-43071569 | Common:1; Rare:85 | ||||
| chr6:43172260-43172451 | Common:1; Rare:35 |