| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:227717983-227718165 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:229921899-229922513 | Common:4; Rare:214 | ||||
| chr2:229923167-229923209 | Rare:13 | ||||
| chr2:230416117-230416270 | Rare:48 | ||||
| chr2:231124997-231125117 | Rare:21 | ||||
| chr2:231460476-231460883 | Common:3; Rare:185 | ||||
| chr2:231464158-231464218 | Rare:17 | ||||
| chr2:231464337-231464684 | Common:3; Rare:120 | ||||
| chr2:231706976-231707194 | Rare:54 | ||||
| chr2:231708480-231708968 | Common:6; Rare:244 | ||||
| chr2:231710278-231710527 | Common:2; Rare:124 | ||||
| chr2:231781247-231781391 | Rare:37 | ||||
| chr2:231961648-231961748 | Rare:29; Clinvar:1 | ||||
| chr2:232550488-232550727 | Rare:96 | ||||
| chr2:232697091-232697375 | Common:2; Rare:94 |