| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:111483214-111483664 | Common:1; Rare:162 | ||||
| chr6:111573701-111573863 | Common:1; Rare:24 | ||||
| chr6:112087409-112087688 | Rare:91 | ||||
| chr6:113857249-113857430 | Common:1; Rare:43 | ||||
| chr6:113970493-113970794 | Common:1; Rare:89 | ||||
| chr6:113971076-113971495 | Common:3; Rare:142 | ||||
| chr6:116100695-116100886 | Rare:69 | ||||
| chr6:116254046-116254251 | Common:4; Rare:58 | ||||
| chr6:116279466-116279632 | Common:1; Rare:55 | ||||
| chr6:116279850-116280108 | Common:2; Rare:86 | ||||
| chr6:116571187-116571569 | Common:2; Rare:107 | ||||
| chr6:116616268-116616494 | Common:3; Rare:47 | ||||
| chr6:116680918-116681337 | Common:4; Rare:124 | ||||
| chr6:118548097-118548350 | Common:2; Rare:52; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:118651591-118651746 | Common:4; Rare:47 |