| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32755238-32755305 | Common:1; Rare:19; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:32755377-32755590 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr12:32755832-32756015 | Rare:68 | ||||
| chr12:39619739-39619899 | Common:1; Rare:28 | ||||
| chr12:42238162-42238462 | Common:1; Rare:98 | ||||
| chr12:42325939-42326227 | Common:1; Rare:90 | ||||
| chr12:43758715-43759013 | Common:2; Rare:88; Clinvar:2 | ||||
| chr12:43806306-43806379 | Common:1; Rare:18 | ||||
| chr12:45215405-45215699 | Common:1; Rare:58 | ||||
| chr12:45215982-45216197 | Common:1; Rare:67 | ||||
| chr12:46268527-46268874 | Common:2; Rare:85 | ||||
| chr12:46268947-46269290 | Common:1; Rare:75 | ||||
| chr12:46362663-46363130 | Common:1; Rare:95 | ||||
| chr12:46364406-46364730 | Common:2; Rare:104 | ||||
| chr12:46365098-46365273 | Common:2; Rare:38 |