| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:132659268-132659621 | Rare:65 | ||||
| chr3:132659799-132659950 | Common:3; Rare:35 | ||||
| chr3:132675058-132675351 | Rare:63; Clinvar (pathogenic):2 | ||||
| chr3:133573481-133573695 | Common:3; Rare:60 | ||||
| chr3:133573815-133574084 | Rare:84 | ||||
| chr3:133661844-133662021 | Rare:42 | ||||
| chr3:134030033-134030230 | Common:2; Rare:38 | ||||
| chr3:134485430-134485896 | Common:1; Rare:117 | ||||
| chr3:134485957-134486253 | Common:3; Rare:105 | ||||
| chr3:134597678-134597857 | Common:1; Rare:22 | ||||
| chr3:134795400-134795540 | Common:1; Rare:35 | ||||
| chr3:135965400-135965730 | Common:1; Rare:117 | ||||
| chr3:136196282-136196668 | Common:1; Rare:142 | ||||
| chr3:136752318-136752716 | Common:1; Rare:128 | ||||
| chr3:136819008-136819121 | Common:2; Rare:61 |