| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10141667-10141870 | Common:1; Rare:93; Clinvar:15; Clinvar (benign):18 | ||||
| chr3:10321038-10321292 | Common:2; Rare:100 | ||||
| chr3:11272190-11272413 | Common:2; Rare:52 | ||||
| chr3:11643818-11644088 | Common:2; Rare:79 | ||||
| chr3:12158902-12158962 | Rare:16 | ||||
| chr3:12484333-12484560 | Common:5; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664064-12664351 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:13420180-13420464 | Common:1; Rare:88 | ||||
| chr3:13480040-13480324 | Common:2; Rare:67 | ||||
| chr3:14124697-14125093 | Common:4; Rare:118; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178876 | Common:2; Rare:163; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402465-14402744 | Common:2; Rare:61 | ||||
| chr3:14651438-14651833 | Rare:119 | ||||
| chr3:14947377-14947554 | Common:3; Rare:88 | ||||
| chr3:15065247-15065454 | Common:5; Rare:67 |