| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:227325182-227325425 | Common:5; Rare:87 | ||||
| chr2:227717981-227718165 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:229805837-229805951 | Rare:22 | ||||
| chr2:229921904-229922513 | Common:4; Rare:210 | ||||
| chr2:230219917-230220067 | Rare:23 | ||||
| chr2:230225633-230225793 | Rare:33 | ||||
| chr2:230416117-230416287 | Rare:53 | ||||
| chr2:230712715-230713140 | Common:5; Rare:141 | ||||
| chr2:230713668-230713930 | Common:1; Rare:72 | ||||
| chr2:230877709-230878188 | Common:2; Rare:99 | ||||
| chr2:231198489-231198742 | Common:1; Rare:82 | ||||
| chr2:231395531-231395812 | Rare:65 | ||||
| chr2:231464152-231464208 | Rare:17 | ||||
| chr2:231464337-231464752 | Common:3; Rare:144 | ||||
| chr2:231707005-231707189 | Rare:42 |