| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49060000-49060907 | Common:1; Rare:647 | ||||
| chr12:49069470-49069860 | Common:15; Rare:278 | ||||
| chr12:49069830-49070360 | Common:14; Rare:492 | ||||
| chr12:49094669-49095076 | Common:3; Rare:225; Clinvar:6; Clinvar (benign):3 | ||||
| chr12:49109408-49110452 | Common:13; Rare:462 | ||||
| chr12:49110530-49111130 | Rare:588 | ||||
| chr12:49130149-49131042 | Common:34; Rare:1156 | ||||
| chr12:49131269-49131820 | Common:14; Rare:972 | ||||
| chr12:49188220-49188670 | Common:7; Rare:240 | ||||
| chr12:49188700-49189089 | Common:5; Rare:157; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264341-49264741 | Common:4; Rare:98 | ||||
| chr12:49264722-49265490 | Common:26; Rare:887 | ||||
| chr12:49265424-49265872 | Common:6; Rare:246 | ||||
| chr12:49297440-49297820 | Common:23; Rare:438; Clinvar:23 | ||||
| chr12:49322847-49323370 | Common:23; Rare:694 |