| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12556949-12557162 | Common:5; Rare:79 | ||||
| chr3:12664075-12664357 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:12759183-12759334 | Common:1; Rare:35 | ||||
| chr3:13420206-13420470 | Common:1; Rare:79 | ||||
| chr3:13480040-13480339 | Common:2; Rare:70 | ||||
| chr3:13548987-13549185 | Common:1; Rare:68 | ||||
| chr3:14017035-14017322 | Common:2; Rare:45 | ||||
| chr3:14124672-14125179 | Common:4; Rare:150; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178471-14178880 | Common:3; Rare:197; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402457-14402722 | Rare:62 | ||||
| chr3:14526195-14526430 | Common:1; Rare:41 | ||||
| chr3:14651486-14651869 | Rare:119 | ||||
| chr3:14947160-14947563 | Common:5; Rare:168 | ||||
| chr3:14948422-14948637 | Common:2; Rare:62 | ||||
| chr3:15206066-15206294 | Common:1; Rare:93 |