| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:230225634-230225779 | Rare:32 | ||||
| chr2:230415750-230416006 | Common:4; Rare:50 | ||||
| chr2:230416098-230416286 | Rare:56 | ||||
| chr2:231395531-231395775 | Rare:59 | ||||
| chr2:231460150-231460566 | Common:1; Rare:146 | ||||
| chr2:231463701-231463814 | Common:2; Rare:31 | ||||
| chr2:231464120-231464232 | Rare:32 | ||||
| chr2:231464337-231464783 | Common:3; Rare:151 | ||||
| chr2:231707000-231707189 | Rare:43 | ||||
| chr2:231708476-231708746 | Common:3; Rare:133 | ||||
| chr2:231708827-231709003 | Common:2; Rare:78 | ||||
| chr2:231710265-231710594 | Common:5; Rare:161 | ||||
| chr2:231781247-231781564 | Common:3; Rare:86 | ||||
| chr2:231786266-231786474 | Common:1; Rare:53 | ||||
| chr2:231961607-231961755 | Rare:52; Clinvar:3 |