| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75334385-75334724 | Common:1; Rare:76 | ||||
| chr12:75390886-75391148 | Common:1; Rare:91 | ||||
| chr12:75511511-75511783 | Rare:89 | ||||
| chr12:76083902-76084316 | Common:1; Rare:123 | ||||
| chr12:76084547-76085072 | Common:6; Rare:145 | ||||
| chr12:76348349-76348508 | Common:1; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559714-76560039 | Common:2; Rare:115 | ||||
| chr12:76764040-76764307 | Common:2; Rare:113 | ||||
| chr12:76764488-76764576 | Rare:34 | ||||
| chr12:76878948-76879141 | Rare:67 | ||||
| chr12:79690471-79690713 | Common:1; Rare:70 | ||||
| chr12:79690882-79691253 | Common:1; Rare:130 | ||||
| chr12:79781814-79782020 | Common:1; Rare:36 | ||||
| chr12:79934791-79935396 | Common:1; Rare:216 | ||||
| chr12:81077780-81078097 | Rare:66 |