| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:131026559-131026940 | Common:2; Rare:85 | ||||
| chr3:131381451-131381837 | Common:3; Rare:107 | ||||
| chr3:131502794-131503004 | Common:1; Rare:93 | ||||
| chr3:132659717-132659989 | Common:3; Rare:64 | ||||
| chr3:133573811-133574005 | Rare:62 | ||||
| chr3:133661928-133662033 | Rare:25 | ||||
| chr3:133746261-133746498 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:134374425-134374727 | Common:2; Rare:94 | ||||
| chr3:134485407-134485772 | Rare:90 | ||||
| chr3:134485957-134486265 | Common:3; Rare:107 | ||||
| chr3:134486429-134486456 | Common:1; Rare:8 | ||||
| chr3:136196298-136196371 | Rare:26 | ||||
| chr3:136250258-136250402 | Common:2; Rare:63; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr3:136752288-136752666 | Common:1; Rare:120 | ||||
| chr3:136862005-136862275 | Common:1; Rare:81 |