| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:186567291-186567431 | Common:3; Rare:37 | ||||
| chr3:186783237-186783638 | Common:2; Rare:177 | ||||
| chr3:187291701-187291864 | Rare:58 | ||||
| chr3:188152886-188153043 | Common:2; Rare:23 | ||||
| chr3:188153763-188154021 | Common:1; Rare:46 | ||||
| chr3:188154060-188154227 | Rare:53 | ||||
| chr3:190322432-190322538 | Common:1; Rare:30 | ||||
| chr3:191329346-191329697 | Common:3; Rare:103 | ||||
| chr3:193593101-193593382 | Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194672153-194672464 | Common:1; Rare:94 | ||||
| chr3:195542980-195543069 | Rare:34 | ||||
| chr3:195543215-195543485 | Common:3; Rare:104 | ||||
| chr3:195720894-195720986 | Common:1; Rare:18 | ||||
| chr3:196318184-196318354 | Common:1; Rare:70 | ||||
| chr3:196432395-196432550 | Common:1; Rare:68 |