| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30881651-30881750 | Common:1; Rare:26 | ||||
| chr22:31081106-31081345 | Common:1; Rare:65 | ||||
| chr22:31107489-31107704 | Common:2; Rare:72 | ||||
| chr22:31212184-31212330 | Rare:54 | ||||
| chr22:31290718-31290911 | Rare:79 | ||||
| chr22:31292425-31292592 | Rare:36 | ||||
| chr22:31399389-31399695 | Common:1; Rare:90 | ||||
| chr22:31496409-31496567 | Common:1; Rare:40 | ||||
| chr22:31749821-31749963 | Common:2; Rare:42 | ||||
| chr22:31750031-31750214 | Common:3; Rare:65 | ||||
| chr22:31753782-31754140 | Common:1; Rare:130 | ||||
| chr22:32412201-32412315 | Common:1; Rare:31 | ||||
| chr22:32474595-32475019 | Common:4; Rare:136; Clinvar:6; Clinvar (benign):2 | ||||
| chr22:32475129-32475337 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr22:32801489-32801710 | Rare:63; Clinvar:3; Clinvar (benign):1 |