| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75390891-75391109 | Common:1; Rare:69 | ||||
| chr12:75480617-75480899 | Rare:61 | ||||
| chr12:75511573-75511680 | Rare:43 | ||||
| chr12:76031593-76031704 | Common:1; Rare:38 | ||||
| chr12:76053089-76053354 | Common:1; Rare:68 | ||||
| chr12:76083928-76084066 | Rare:42 | ||||
| chr12:76348351-76348480 | Common:1; Rare:50; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559534-76559909 | Common:2; Rare:125 | ||||
| chr12:76764040-76764276 | Common:2; Rare:97 | ||||
| chr12:76846530-76846675 | Rare:33 | ||||
| chr12:76879012-76879269 | Rare:80 | ||||
| chr12:79690506-79690639 | Rare:36 | ||||
| chr12:79690938-79691225 | Common:1; Rare:93 | ||||
| chr12:79934713-79935288 | Common:1; Rare:198 | ||||
| chr12:79935323-79935396 | Rare:19 |