| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33718050-33718266 | Rare:72 | ||||
| chr3:33798484-33798701 | Common:2; Rare:78 | ||||
| chr3:35638820-35638951 | Rare:28 | ||||
| chr3:35639427-35640106 | Common:6; Rare:153 | ||||
| chr3:35642152-35642254 | Rare:16 | ||||
| chr3:35642275-35642389 | Rare:19 | ||||
| chr3:35643471-35643651 | Rare:33 | ||||
| chr3:36993040-36993553 | Common:2; Rare:174; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr3:36993717-36993842 | Rare:48; Clinvar:1 | ||||
| chr3:37176084-37176387 | Common:1; Rare:84 | ||||
| chr3:37243166-37243364 | Common:1; Rare:50 | ||||
| chr3:38024510-38024664 | Common:1; Rare:57 | ||||
| chr3:38029597-38029924 | Common:2; Rare:63 | ||||
| chr3:38138624-38138675 | Common:1; Rare:21 | ||||
| chr3:38165013-38165217 | Common:1; Rare:42 |