| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:112087409-112087690 | Rare:91 | ||||
| chr6:113970327-113970412 | Rare:31 | ||||
| chr6:113970599-113970810 | Rare:66 | ||||
| chr6:113970888-113971027 | Common:2; Rare:69 | ||||
| chr6:116100680-116100913 | Common:1; Rare:93 | ||||
| chr6:116253991-116254247 | Common:5; Rare:78 | ||||
| chr6:116279841-116280120 | Common:2; Rare:94 | ||||
| chr6:116370735-116371023 | Rare:73 | ||||
| chr6:116571170-116571595 | Common:3; Rare:123 | ||||
| chr6:116616289-116616487 | Common:3; Rare:41 | ||||
| chr6:116680891-116681303 | Common:4; Rare:126 | ||||
| chr6:117602192-117602272 | Rare:40 | ||||
| chr6:117602471-117602677 | Common:3; Rare:57 | ||||
| chr6:117675318-117675498 | Common:3; Rare:49 | ||||
| chr6:118548195-118548365 | Common:2; Rare:37; Clinvar:3; Clinvar (benign):2 |