| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:111483700-111483775 | Common:1; Rare:34 | ||||
| chr6:111605950-111605968 | Rare:5 | ||||
| chr6:111606060-111606150 | Rare:20 | ||||
| chr6:112087198-112087719 | Common:1; Rare:171 | ||||
| chr6:112139243-112139448 | Common:2; Rare:37; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:113857036-113857351 | Common:1; Rare:77 | ||||
| chr6:113968499-113968785 | Common:3; Rare:42 | ||||
| chr6:113969733-113970002 | Common:1; Rare:48 | ||||
| chr6:113970142-113970292 | Rare:35 | ||||
| chr6:113970583-113970813 | Rare:69 | ||||
| chr6:113970881-113971063 | Common:2; Rare:82 | ||||
| chr6:113971076-113971512 | Common:3; Rare:143 | ||||
| chr6:116100680-116100951 | Common:1; Rare:111 | ||||
| chr6:116253353-116253642 | Rare:83 | ||||
| chr6:116253654-116253732 | Rare:27 |