| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127672805-127673011 | Common:3; Rare:99 | ||||
| chr3:128052139-128052558 | Common:4; Rare:143 | ||||
| chr3:128153365-128153487 | Rare:33 | ||||
| chr3:128487917-128488139 | Rare:56 | ||||
| chr3:128726084-128726387 | Common:3; Rare:94; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:128879404-128879685 | Common:4; Rare:139; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:129160974-129161152 | Common:1; Rare:67 | ||||
| chr3:129183778-129184080 | Common:2; Rare:102 | ||||
| chr3:129249503-129249744 | Common:3; Rare:66 | ||||
| chr3:129316279-129316399 | Common:1; Rare:34 | ||||
| chr3:129439735-129440355 | Common:1; Rare:189; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129560522-129560663 | Rare:29 | ||||
| chr3:129893580-129893891 | Rare:133 | ||||
| chr3:130746744-130746954 | Common:3; Rare:62 | ||||
| chr3:130893885-130894245 | Common:3; Rare:110 |