| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132687252-132687713 | Common:4; Rare:170; Clinvar:14; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr12:132710537-132711061 | Common:5; Rare:164 | ||||
| chr12:132828820-132829255 | Common:4; Rare:164 | ||||
| chr12:132887548-132887899 | Rare:100 | ||||
| chr12:132956136-132956431 | Common:1; Rare:61 | ||||
| chr12:132986221-132986464 | Rare:63 | ||||
| chr12:133037220-133037542 | Common:4; Rare:66 | ||||
| chr12:133080180-133080454 | Common:7; Rare:87 | ||||
| chr12:133080506-133081033 | Common:4; Rare:162 | ||||
| chr12:133130218-133130662 | Common:7; Rare:150 | ||||
| chr12:133181348-133181581 | Common:2; Rare:73 | ||||
| chr13:19633355-19633774 | Common:1; Rare:153 | ||||
| chr13:19782918-19783094 | Common:2; Rare:62 | ||||
| chr13:19863441-19863838 | Common:5; Rare:133 | ||||
| chr13:19958462-19958757 | Common:5; Rare:142 |