| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6534270-6534568 | Common:5; Rare:125 | ||||
| chr12:6536427-6537009 | Rare:213 | ||||
| chr12:6568260-6568388 | Rare:50 | ||||
| chr12:6606422-6606717 | Common:3; Rare:102 | ||||
| chr12:6688870-6689195 | Rare:101 | ||||
| chr12:6689445-6689748 | Common:2; Rare:76 | ||||
| chr12:6723807-6724158 | Common:1; Rare:70 | ||||
| chr12:6724196-6724291 | Rare:21 | ||||
| chr12:6766386-6766748 | Rare:108 | ||||
| chr12:6851902-6852174 | Rare:70 | ||||
| chr12:6867381-6867645 | Common:2; Rare:132; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868863-6869141 | Rare:87; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:6873274-6873541 | Common:2; Rare:77 | ||||
| chr12:6914406-6914621 | Rare:55 | ||||
| chr12:6927548-6927834 | Rare:74 |