| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:229921297-229921463 | Common:2; Rare:39 | ||||
| chr2:229921904-229922507 | Common:4; Rare:205 | ||||
| chr2:229923167-229923370 | Common:1; Rare:47 | ||||
| chr2:231198526-231198666 | Common:1; Rare:47 | ||||
| chr2:231464142-231464222 | Rare:23 | ||||
| chr2:231464337-231464792 | Common:3; Rare:155 | ||||
| chr2:231707011-231707203 | Rare:45 | ||||
| chr2:231708359-231708666 | Common:3; Rare:141 | ||||
| chr2:231708673-231708745 | Rare:30 | ||||
| chr2:231710278-231710527 | Common:2; Rare:124 | ||||
| chr2:231781206-231781426 | Rare:64 | ||||
| chr2:231961628-231961748 | Rare:37; Clinvar:2 | ||||
| chr2:232550527-232550721 | Rare:78 | ||||
| chr2:232776530-232776738 | Rare:37; Clinvar:1 | ||||
| chr2:233060273-233060364 | Rare:14 |