| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:82358727-82358899 | Common:3; Rare:89 | ||||
| chr12:82686712-82686929 | Rare:72 | ||||
| chr12:85036234-85036362 | Rare:30 | ||||
| chr12:88035433-88035587 | Common:1; Rare:47 | ||||
| chr12:88142032-88142394 | Rare:100; Clinvar:3 | ||||
| chr12:88580409-88580556 | Common:2; Rare:53 | ||||
| chr12:89352398-89352661 | Rare:69 | ||||
| chr12:89353668-89353744 | Common:3; Rare:19 | ||||
| chr12:89524557-89524599 | Rare:17 | ||||
| chr12:89524748-89524869 | Common:1; Rare:22 | ||||
| chr12:89525885-89525951 | Common:1; Rare:21 | ||||
| chr12:89525977-89526073 | Rare:38 | ||||
| chr12:89708819-89709050 | Common:1; Rare:89 | ||||
| chr12:91180667-91180903 | Common:2; Rare:28 | ||||
| chr12:91182653-91183141 | Common:1; Rare:91; Clinvar:3; Clinvar (benign):3 |