| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75390893-75391103 | Common:1; Rare:62 | ||||
| chr12:75480587-75480949 | Rare:79 | ||||
| chr12:76030508-76031355 | Common:5; Rare:325 | ||||
| chr12:76031593-76031879 | Common:1; Rare:89 | ||||
| chr12:76084566-76085086 | Common:6; Rare:143 | ||||
| chr12:76348342-76348531 | Common:1; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559591-76559924 | Common:2; Rare:116 | ||||
| chr12:76763936-76764281 | Common:4; Rare:145 | ||||
| chr12:76878948-76879214 | Rare:94 | ||||
| chr12:79934771-79935269 | Common:1; Rare:175 | ||||
| chr12:79935342-79935363 | Rare:4 | ||||
| chr12:80937688-80937803 | Common:1; Rare:34 | ||||
| chr12:82358366-82358555 | Rare:80 | ||||
| chr12:82358727-82358891 | Common:3; Rare:85 | ||||
| chr12:84912720-84912912 | Common:1; Rare:46 |