| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:125990557-125990586 | Rare:7 | ||||
| chr3:128486269-128486532 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:130111461-130111776 | Common:3; Rare:75 | ||||
| chr3:130112406-130112589 | Common:3; Rare:56 | ||||
| chr3:131361588-131361904 | Common:3; Rare:96 | ||||
| chr3:136625262-136625398 | Rare:31 | ||||
| chr3:139354600-139354644 | Common:1; Rare:4 | ||||
| chr3:141311708-141311876 | Common:1; Rare:48 | ||||
| chr3:150408837-150409163 | Rare:87 | ||||
| chr3:150581493-150581719 | Rare:55 | ||||
| chr3:155141921-155142306 | Rare:122; Clinvar:1 | ||||
| chr3:155158534-155158840 | Common:3; Rare:55 | ||||
| chr3:157174932-157175275 | Common:3; Rare:154 | ||||
| chr3:159732263-159732396 | Common:1; Rare:24 | ||||
| chr3:159763071-159763147 | Rare:18 |