| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:16611248-16611430 | Rare:30 | ||||
| chr12:16726969-16727112 | Common:1; Rare:25 | ||||
| chr12:17167762-17167893 | Common:1; Rare:23 | ||||
| chr12:17370001-17370078 | Common:2; Rare:13 | ||||
| chr12:17370781-17370935 | Common:1; Rare:24 | ||||
| chr12:17371533-17371647 | Rare:17 | ||||
| chr12:17371970-17372015 | Rare:14 | ||||
| chr12:17372037-17372198 | Common:2; Rare:20 | ||||
| chr12:17372608-17372829 | Rare:34 | ||||
| chr12:17388653-17388667 | Rare:2 | ||||
| chr12:17579767-17579791 | Rare:5 | ||||
| chr12:17587512-17587579 | Rare:13 | ||||
| chr12:17587782-17587796 | Rare:3 | ||||
| chr12:17587878-17588020 | Common:2; Rare:25 | ||||
| chr12:17588597-17588624 | Rare:2 |