| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10141650-10141870 | Common:3; Rare:97; Clinvar:15; Clinvar (benign):19 | ||||
| chr3:10142140-10142185 | Rare:17; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr3:10321038-10321286 | Common:2; Rare:98 | ||||
| chr3:10992232-10992256 | Rare:3 | ||||
| chr3:11272220-11272437 | Common:2; Rare:49 | ||||
| chr3:11719419-11719595 | Rare:57 | ||||
| chr3:12004215-12004408 | Common:3; Rare:57 | ||||
| chr3:12484181-12484804 | Common:9; Rare:177; Clinvar:10; Clinvar (benign):4 | ||||
| chr3:12556920-12557153 | Common:5; Rare:85 | ||||
| chr3:12663819-12663913 | Rare:25; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:12664075-12664371 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:12796596-12796733 | Common:3; Rare:47 | ||||
| chr3:13073407-13073582 | Common:5; Rare:57 | ||||
| chr3:13420192-13420466 | Common:1; Rare:85 | ||||
| chr3:13480040-13480330 | Common:2; Rare:67 |