| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:227871606-227871678 | Common:2; Rare:29 | ||||
| chr2:228181611-228181778 | Rare:50 | ||||
| chr2:229921924-229922522 | Common:3; Rare:210 | ||||
| chr2:230864381-230865055 | Common:9; Rare:157 | ||||
| chr2:231198352-231198690 | Common:2; Rare:116 | ||||
| chr2:231464142-231464219 | Rare:22 | ||||
| chr2:231464376-231464735 | Common:3; Rare:125 | ||||
| chr2:231706950-231707199 | Rare:63 | ||||
| chr2:231707407-231707581 | Rare:46 | ||||
| chr2:231708359-231708746 | Common:3; Rare:175 | ||||
| chr2:231710289-231710527 | Common:2; Rare:115 | ||||
| chr2:231786155-231786481 | Common:3; Rare:88 | ||||
| chr2:231961621-231961755 | Rare:44; Clinvar:2 | ||||
| chr2:232550533-232550723 | Rare:77 | ||||
| chr2:232697130-232697379 | Common:2; Rare:81 |