| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129249453-129249742 | Common:8; Rare:196 | ||||
| chr3:129278060-129278650 | Common:7; Rare:163 | ||||
| chr3:129278662-129279109 | Common:12; Rare:306 | ||||
| chr3:129315479-129315880 | Common:6; Rare:278 | ||||
| chr3:129316058-129316411 | Common:9; Rare:315 | ||||
| chr3:129316560-129316930 | Common:12; Rare:160 | ||||
| chr3:129428500-129428880 | Common:6; Rare:177 | ||||
| chr3:129439032-129439673 | Common:2; Rare:126 | ||||
| chr3:129439729-129440501 | Common:11; Rare:624; Clinvar:9; Clinvar (benign):3 | ||||
| chr3:129440522-129440697 | Rare:45 | ||||
| chr3:129487773-129488255 | Common:10; Rare:212 | ||||
| chr3:129495078-129495394 | Rare:43 | ||||
| chr3:129606399-129607046 | Common:14; Rare:346 | ||||
| chr3:129607098-129607498 | Common:2; Rare:105 | ||||
| chr3:129892747-129893045 | Common:1; Rare:67 |