| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132687288-132687696 | Common:4; Rare:151; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710722-132710852 | Common:3; Rare:60 | ||||
| chr12:132828830-132829160 | Common:4; Rare:112 | ||||
| chr12:132887553-132887860 | Rare:91 | ||||
| chr12:132956252-132956443 | Common:1; Rare:40 | ||||
| chr12:132986235-132986423 | Rare:41 | ||||
| chr12:133037216-133037543 | Common:4; Rare:68 | ||||
| chr12:133080123-133080459 | Common:7; Rare:106 | ||||
| chr12:133130218-133130652 | Common:7; Rare:145 | ||||
| chr12:133181364-133181567 | Common:2; Rare:61 | ||||
| chr13:19633430-19633746 | Common:1; Rare:118 | ||||
| chr13:19782921-19783090 | Common:2; Rare:60 | ||||
| chr13:19863441-19863600 | Common:1; Rare:44 | ||||
| chr13:19863636-19863840 | Common:2; Rare:74 | ||||
| chr13:19958962-19959088 | Common:2; Rare:47 |