| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792246-9792628 | Common:2; Rare:451 | ||||
| chr3:9792624-9793178 | Common:21; Rare:1050 | ||||
| chr3:9793508-9793657 | Rare:53 | ||||
| chr3:9843923-9844248 | Common:14; Rare:497 | ||||
| chr3:9890344-9891958 | Common:27; Rare:1181; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr3:9902380-9902839 | Common:6; Rare:194 | ||||
| chr3:9902814-9903214 | Common:1; Rare:118 | ||||
| chr3:9903350-9903750 | Common:2; Rare:243 | ||||
| chr3:9916620-9917350 | Common:14; Rare:296; Clinvar (benign):1 | ||||
| chr3:9933172-9933957 | Common:17; Rare:1066; Clinvar:16; Clinvar (benign):6 | ||||
| chr3:9933910-9934150 | Rare:168 | ||||
| chr3:9934172-9934572 | Common:3; Rare:128; Clinvar (benign):1 | ||||
| chr3:9951922-9952394 | Common:6; Rare:136 | ||||
| chr3:9952321-9952801 | Common:1; Rare:118 | ||||
| chr3:9986396-9987367 | Common:37; Rare:1030 |