| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:36993108-36993539 | Common:2; Rare:135; Clinvar:25; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr3:37243116-37243369 | Common:3; Rare:69 | ||||
| chr3:37987878-37987994 | Rare:17 | ||||
| chr3:39051944-39052036 | Common:1; Rare:35 | ||||
| chr3:39107562-39107680 | Common:2; Rare:39 | ||||
| chr3:39383588-39383676 | Rare:20; Clinvar:1 | ||||
| chr3:39406605-39406736 | Common:2; Rare:45 | ||||
| chr3:40309479-40309808 | Common:9; Rare:112 | ||||
| chr3:40457204-40457381 | Common:3; Rare:86 | ||||
| chr3:42581907-42582132 | Common:3; Rare:69 | ||||
| chr3:42600425-42600716 | Common:2; Rare:110 | ||||
| chr3:42804434-42804691 | Common:2; Rare:85 | ||||
| chr3:43286459-43286623 | Common:1; Rare:76 | ||||
| chr3:43621968-43622316 | Common:2; Rare:96; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:43690760-43690947 | Common:1; Rare:87; Clinvar:5; Clinvar (benign):1 |