| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76031593-76031820 | Common:1; Rare:81 | ||||
| chr12:76083912-76084076 | Rare:49 | ||||
| chr12:76348342-76348468 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559653-76559884 | Rare:85 | ||||
| chr12:76764040-76764269 | Common:2; Rare:94 | ||||
| chr12:76878982-76879206 | Rare:78 | ||||
| chr12:79934888-79935286 | Common:1; Rare:153 | ||||
| chr12:79935329-79935388 | Rare:15 | ||||
| chr12:80937679-80937859 | Common:1; Rare:56 | ||||
| chr12:81077752-81078172 | Rare:97 | ||||
| chr12:82358329-82358568 | Rare:113 | ||||
| chr12:82358736-82358905 | Common:3; Rare:86 | ||||
| chr12:82686786-82686919 | Rare:44 | ||||
| chr12:84912720-84912897 | Common:1; Rare:42 | ||||
| chr12:88142032-88142390 | Rare:98; Clinvar:3 |