| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14402437-14402722 | Rare:65 | ||||
| chr3:14651468-14651807 | Rare:99 | ||||
| chr3:14947236-14947605 | Common:4; Rare:164 | ||||
| chr3:14948022-14948340 | Rare:142 | ||||
| chr3:14948354-14948641 | Common:2; Rare:81 | ||||
| chr3:15205957-15206294 | Common:1; Rare:124 | ||||
| chr3:15341377-15341585 | Rare:35 | ||||
| chr3:15427471-15427711 | Common:1; Rare:81 | ||||
| chr3:15601476-15601810 | Common:4; Rare:141; Clinvar:2 | ||||
| chr3:15601859-15602010 | Common:1; Rare:76; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:15797286-15797362 | Rare:9 | ||||
| chr3:15859505-15859691 | Common:4; Rare:51 | ||||
| chr3:15859782-15860114 | Common:4; Rare:104 | ||||
| chr3:16174400-16175095 | Common:2; Rare:140 | ||||
| chr3:16175232-16175631 | Common:3; Rare:127 |