| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75390891-75391109 | Common:1; Rare:69 | ||||
| chr12:76083934-76084085 | Rare:45 | ||||
| chr12:76084547-76084872 | Common:1; Rare:106 | ||||
| chr12:76085049-76085052 | |||||
| chr12:76085157-76085327 | Common:1; Rare:46 | ||||
| chr12:76348351-76348545 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76422626-76422822 | Rare:51 | ||||
| chr12:76559494-76559909 | Common:2; Rare:135 | ||||
| chr12:76764040-76764307 | Common:2; Rare:113 | ||||
| chr12:76878942-76879127 | Rare:61 | ||||
| chr12:78864314-78864388 | Common:1; Rare:10 | ||||
| chr12:78864572-78865104 | Common:2; Rare:116 | ||||
| chr12:79934886-79935355 | Common:1; Rare:180 | ||||
| chr12:80937679-80937809 | Common:1; Rare:39 | ||||
| chr12:80937914-80938304 | Common:2; Rare:74 |