| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75390880-75391109 | Common:1; Rare:70 | ||||
| chr12:76053090-76053360 | Common:1; Rare:72 | ||||
| chr12:76083920-76084041 | Rare:39 | ||||
| chr12:76084543-76084799 | Common:1; Rare:87 | ||||
| chr12:76348351-76348452 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559702-76559919 | Rare:83 | ||||
| chr12:76764040-76764277 | Common:2; Rare:98 | ||||
| chr12:76878947-76879145 | Rare:68 | ||||
| chr12:79690520-79690625 | Rare:25 | ||||
| chr12:79934713-79935310 | Common:1; Rare:211 | ||||
| chr12:79935335-79935406 | Rare:17 | ||||
| chr12:80937679-80937809 | Common:1; Rare:39 | ||||
| chr12:80937932-80938109 | Common:1; Rare:29 | ||||
| chr12:81077973-81078157 | Rare:42 | ||||
| chr12:82358273-82358579 | Common:1; Rare:152 |