| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:13420212-13420466 | Common:1; Rare:76 | ||||
| chr3:13480040-13480418 | Common:3; Rare:86 | ||||
| chr3:13549014-13549196 | Rare:62 | ||||
| chr3:14124678-14125184 | Common:4; Rare:149; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178467-14178880 | Common:3; Rare:199; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402437-14402776 | Common:4; Rare:72 | ||||
| chr3:14651486-14651824 | Rare:101 | ||||
| chr3:14947166-14947605 | Common:5; Rare:181 | ||||
| chr3:14948019-14948208 | Rare:85 | ||||
| chr3:14948363-14948637 | Common:2; Rare:73 | ||||
| chr3:15065121-15065369 | Common:2; Rare:89 | ||||
| chr3:15099115-15099299 | Rare:46 | ||||
| chr3:15206019-15206337 | Common:1; Rare:116 | ||||
| chr3:15427431-15427679 | Common:1; Rare:81 | ||||
| chr3:15601502-15601815 | Common:4; Rare:131; Clinvar:2 |