| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191571289-191571325 | Common:1; Rare:7 | ||||
| chr2:191625173-191625400 | Rare:29 | ||||
| chr2:191675904-191676016 | Common:1; Rare:18 | ||||
| chr2:191677389-191677486 | Common:1; Rare:7 | ||||
| chr2:191680282-191680375 | Common:2; Rare:18 | ||||
| chr2:191715427-191715560 | Rare:26 | ||||
| chr2:191728910-191729172 | Common:2; Rare:33 | ||||
| chr2:191738771-191738892 | Common:1; Rare:16 | ||||
| chr2:191758544-191758646 | Common:2; Rare:16 | ||||
| chr2:191759062-191759173 | Rare:28 | ||||
| chr2:191910509-191910727 | Common:1; Rare:40 | ||||
| chr2:192161810-192161977 | Rare:22 | ||||
| chr2:192687080-192687259 | Rare:32 | ||||
| chr2:192751527-192751562 | Rare:6 | ||||
| chr2:195251322-195251587 | Common:1; Rare:33 |