| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48904021-48904159 | Common:2; Rare:31 | ||||
| chr12:48925481-48925735 | Common:2; Rare:52 | ||||
| chr12:48939740-48940033 | Common:2; Rare:69 | ||||
| chr12:48956428-48956703 | Common:3; Rare:51 | ||||
| chr12:49003508-49003834 | Common:1; Rare:90 | ||||
| chr12:49018733-49019037 | Common:1; Rare:112; Clinvar (benign):1 | ||||
| chr12:49131317-49131606 | Common:2; Rare:117 | ||||
| chr12:49188443-49188607 | Common:2; Rare:23 | ||||
| chr12:49188875-49189152 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264729-49265170 | Common:5; Rare:159 | ||||
| chr12:49269652-49269771 | Rare:35 | ||||
| chr12:49367248-49367582 | Common:1; Rare:88 | ||||
| chr12:49567843-49568243 | Common:2; Rare:109 | ||||
| chr12:49623250-49623581 | Common:1; Rare:94 | ||||
| chr12:49758225-49758480 | Common:4; Rare:79 |