| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:45014165-45014313 | Common:4; Rare:39 | ||||
| chr2:45170004-45170088 | Rare:22 | ||||
| chr2:45180103-45180314 | Common:1; Rare:41 | ||||
| chr2:45610539-45610702 | Rare:40 | ||||
| chr2:45643720-45643848 | Common:2; Rare:40 | ||||
| chr2:45938891-45938968 | Common:2; Rare:18 | ||||
| chr2:45944326-45944355 | Rare:6 | ||||
| chr2:46500244-46500333 | Common:1; Rare:22 | ||||
| chr2:46749095-46749386 | Common:2; Rare:48 | ||||
| chr2:47056578-47056730 | Common:2; Rare:33 | ||||
| chr2:47175527-47175769 | Common:1; Rare:80 | ||||
| chr2:47177163-47177352 | Rare:56 | ||||
| chr2:47191532-47191643 | Rare:27 | ||||
| chr2:47192545-47192605 | Rare:13 | ||||
| chr2:47192893-47192959 | Common:2; Rare:15 |