| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:11650033-11650124 | Rare:28 | ||||
| chr12:11650328-11650377 | Common:3; Rare:8 | ||||
| chr12:12135227-12135367 | Rare:53 | ||||
| chr12:12357001-12357137 | Common:1; Rare:72 | ||||
| chr12:12611590-12612064 | Common:2; Rare:133 | ||||
| chr12:12612100-12612172 | Common:1; Rare:22 | ||||
| chr12:12717467-12717772 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:12725651-12726008 | Common:3; Rare:78 | ||||
| chr12:12890638-12890809 | Common:1; Rare:31 | ||||
| chr12:12891228-12891814 | Common:3; Rare:111 | ||||
| chr12:13000199-13000476 | Common:2; Rare:90 | ||||
| chr12:13196236-13196616 | Common:1; Rare:65 | ||||
| chr12:13197027-13197170 | Common:1; Rare:20 | ||||
| chr12:13197263-13197467 | Common:1; Rare:37 | ||||
| chr12:13213062-13213243 | Common:1; Rare:33 |