| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215371640-215371943 | Common:4; Rare:60 | ||||
| chr2:215435650-215435808 | Common:2; Rare:45 | ||||
| chr2:215435810-215436107 | Common:1; Rare:68 | ||||
| chr2:215436111-215436307 | Common:1; Rare:66 | ||||
| chr2:216081761-216081925 | Common:1; Rare:58 | ||||
| chr2:216412670-216412788 | Rare:14 | ||||
| chr2:216498679-216498886 | Common:6; Rare:81 | ||||
| chr2:216499022-216499323 | Common:4; Rare:68 | ||||
| chr2:216694437-216695208 | Common:1; Rare:163 | ||||
| chr2:216695219-216695452 | Common:1; Rare:39 | ||||
| chr2:216695469-216695590 | Rare:24 | ||||
| chr2:218216812-218217299 | Common:3; Rare:134 | ||||
| chr2:218270091-218270532 | Common:5; Rare:137; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218568316-218568913 | Common:5; Rare:146 | ||||
| chr2:218659591-218659799 | Rare:58 |