| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71839593-71839804 | Common:1; Rare:80 | ||||
| chr12:74537707-74537873 | Common:1; Rare:62 | ||||
| chr12:76031119-76031326 | Common:4; Rare:80 | ||||
| chr12:76031593-76031813 | Common:1; Rare:78 | ||||
| chr12:76083915-76084038 | Rare:40 | ||||
| chr12:76084566-76084897 | Common:2; Rare:115 | ||||
| chr12:76348360-76348468 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76764040-76764261 | Common:2; Rare:91 | ||||
| chr12:76878987-76879182 | Rare:67 | ||||
| chr12:77065504-77065774 | Common:1; Rare:90 | ||||
| chr12:78863915-78863998 | Rare:21 | ||||
| chr12:79934753-79935396 | Common:1; Rare:223 | ||||
| chr12:82358322-82358556 | Rare:110 | ||||
| chr12:82358721-82358899 | Common:3; Rare:93 | ||||
| chr12:88035412-88035589 | Common:1; Rare:49 |