| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4829534-4829747 | Common:2; Rare:30 | ||||
| chr12:4943702-4943913 | Rare:29 | ||||
| chr12:6167308-6167473 | Common:1; Rare:31 | ||||
| chr12:6278049-6278329 | Rare:47 | ||||
| chr12:6330094-6330394 | Common:4; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6335740-6335967 | Common:1; Rare:48 | ||||
| chr12:6336689-6336821 | Common:1; Rare:22 | ||||
| chr12:6337365-6337472 | Rare:23 | ||||
| chr12:6426961-6427210 | Rare:33 | ||||
| chr12:6427474-6427628 | Common:1; Rare:21 | ||||
| chr12:6430538-6430653 | Rare:19 | ||||
| chr12:6433185-6433217 | Rare:5 | ||||
| chr12:6443531-6443670 | Common:1; Rare:21 | ||||
| chr12:6446340-6446625 | Common:1; Rare:35 | ||||
| chr12:6446912-6447056 | Rare:28 |