| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128153708-128154120 | Common:7; Rare:199 | ||||
| chr3:128487790-128488133 | Common:4; Rare:201 | ||||
| chr3:128488492-128488657 | Common:2; Rare:67 | ||||
| chr3:128649900-128650440 | Common:6; Rare:150 | ||||
| chr3:128650430-128651011 | Common:6; Rare:474 | ||||
| chr3:128680620-128681393 | Common:10; Rare:463 | ||||
| chr3:128725869-128726322 | Common:5; Rare:274; Clinvar:11; Clinvar (benign):5 | ||||
| chr3:128726690-128727180 | Common:2; Rare:109 | ||||
| chr3:128879333-128879775 | Common:14; Rare:528; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr3:128994040-128994233 | Common:2; Rare:114 | ||||
| chr3:129001450-129001640 | Common:2; Rare:52 | ||||
| chr3:129120804-129122103 | Common:11; Rare:418 | ||||
| chr3:129160973-129161533 | Common:10; Rare:434 | ||||
| chr3:129161650-129161841 | Common:1; Rare:45 | ||||
| chr3:129183695-129184326 | Common:8; Rare:474 |