| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45183473-45183565 | Rare:15 | ||||
| chr3:45200110-45200357 | Common:6; Rare:48 | ||||
| chr3:45442082-45442317 | Rare:41 | ||||
| chr3:45508159-45508327 | Common:1; Rare:27 | ||||
| chr3:45509082-45509426 | Common:4; Rare:49 | ||||
| chr3:45509518-45509642 | Rare:8 | ||||
| chr3:45593322-45593476 | Common:4; Rare:25 | ||||
| chr3:45677253-45677409 | Common:1; Rare:21 | ||||
| chr3:46558491-46558648 | Common:2; Rare:34 | ||||
| chr3:46629963-46630043 | Rare:13 | ||||
| chr3:46845515-46845702 | Common:3; Rare:31 | ||||
| chr3:46845884-46846269 | Common:3; Rare:89 | ||||
| chr3:46874597-46874803 | Common:3; Rare:58 | ||||
| chr3:47009279-47009724 | Common:5; Rare:159; Clinvar:5; Clinvar (benign):4 | ||||
| chr3:47009930-47010004 | Rare:11 |