| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:15627413-15627503 | Rare:31; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:15754446-15754683 | Common:1; Rare:40 | ||||
| chr6:16131102-16131236 | Rare:22 | ||||
| chr6:16320058-16320421 | Common:2; Rare:78 | ||||
| chr6:16322773-16322997 | Rare:37 | ||||
| chr6:16337807-16337929 | Rare:17 | ||||
| chr6:16345667-16345888 | Rare:44 | ||||
| chr6:16345907-16346004 | Rare:28 | ||||
| chr6:16669217-16669537 | Common:2; Rare:49 | ||||
| chr6:16683847-16684114 | Common:3; Rare:49 | ||||
| chr6:16685332-16685476 | Rare:26 | ||||
| chr6:16712365-16712659 | Common:3; Rare:44 | ||||
| chr6:16712777-16713015 | Rare:38 | ||||
| chr6:16713059-16713212 | Common:1; Rare:23 | ||||
| chr6:16713235-16713520 | Rare:46 |