| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127822684-127823014 | Common:1; Rare:109 | ||||
| chr3:127823124-127823428 | Common:4; Rare:67 | ||||
| chr3:128051875-128052021 | Rare:43 | ||||
| chr3:128052062-128052536 | Common:4; Rare:151 | ||||
| chr3:128123752-128124187 | Rare:123 | ||||
| chr3:128153154-128153241 | Rare:23 | ||||
| chr3:128153305-128153499 | Common:2; Rare:52 | ||||
| chr3:128153735-128154022 | Common:3; Rare:79 | ||||
| chr3:128650195-128650380 | Common:3; Rare:51 | ||||
| chr3:128650724-128651151 | Common:3; Rare:124 | ||||
| chr3:128680628-128680966 | Common:3; Rare:106 | ||||
| chr3:128680982-128681257 | Common:1; Rare:70 | ||||
| chr3:128726006-128726265 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:128879346-128879713 | Common:5; Rare:171; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129121762-129122090 | Common:1; Rare:57 |