| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:130999517-130999836 | Common:2; Rare:49; Clinvar (benign):1 | ||||
| chr3:131361595-131361697 | Common:1; Rare:33 | ||||
| chr3:132136021-132136260 | Rare:46 | ||||
| chr3:132434303-132434619 | Common:4; Rare:86 | ||||
| chr3:133586679-133586919 | Rare:59 | ||||
| chr3:133735359-133735427 | Rare:8 | ||||
| chr3:134201255-134201539 | Rare:57 | ||||
| chr3:134327009-134327203 | Rare:32 | ||||
| chr3:134328259-134328510 | Rare:56 | ||||
| chr3:134385634-134385680 | Rare:5 | ||||
| chr3:134484900-134484988 | Rare:14 | ||||
| chr3:136108457-136108704 | Common:1; Rare:48 | ||||
| chr3:136195277-136195339 | Rare:15 | ||||
| chr3:136332331-136332435 | Rare:15 | ||||
| chr3:136840474-136840586 | Common:2; Rare:27 |