| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:132659771-132659950 | Common:3; Rare:44 | ||||
| chr3:132722144-132722204 | Common:1; Rare:28; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:133573830-133573994 | Rare:48 | ||||
| chr3:133661844-133662004 | Rare:37 | ||||
| chr3:134374405-134374655 | Common:1; Rare:72 | ||||
| chr3:134485488-134485766 | Rare:68 | ||||
| chr3:134485957-134486208 | Common:2; Rare:86 | ||||
| chr3:136196299-136196614 | Common:1; Rare:115 | ||||
| chr3:136752349-136752677 | Common:1; Rare:110 | ||||
| chr3:136862016-136862306 | Common:1; Rare:90 | ||||
| chr3:138174883-138174960 | Common:1; Rare:15 | ||||
| chr3:138187281-138187569 | Rare:81 | ||||
| chr3:138594209-138594442 | Rare:65 | ||||
| chr3:138608880-138609081 | Rare:51 | ||||
| chr3:138834874-138835010 | Rare:40 |