| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:130839129-130839394 | Common:2; Rare:94 | ||||
| chr12:130871668-130872126 | Common:4; Rare:187 | ||||
| chr12:130953775-130954016 | Rare:46 | ||||
| chr12:130954155-130954277 | Rare:22 | ||||
| chr12:130993917-130994226 | Rare:100 | ||||
| chr12:131710759-131711119 | Rare:103 | ||||
| chr12:131929000-131929308 | Common:10; Rare:95; Clinvar:1 | ||||
| chr12:131949655-131950010 | Common:2; Rare:121 | ||||
| chr12:132084061-132084338 | Common:6; Rare:98 | ||||
| chr12:132687291-132687707 | Common:4; Rare:156; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710532-132711061 | Common:5; Rare:165 | ||||
| chr12:132829017-132829251 | Rare:102 | ||||
| chr12:132887553-132887868 | Rare:93 | ||||
| chr12:132956252-132956383 | Common:1; Rare:31 | ||||
| chr12:132986236-132986470 | Rare:56 |