| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132490754-132490906 | Rare:34 | ||||
| chr5:132556816-132557037 | Common:1; Rare:77; Clinvar:1 | ||||
| chr5:132737476-132737743 | Rare:85 | ||||
| chr5:132777233-132777469 | Rare:59 | ||||
| chr5:132777584-132778048 | Common:1; Rare:93 | ||||
| chr5:132830510-132831080 | Common:1; Rare:159 | ||||
| chr5:132866421-132866711 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963584-132963844 | Common:1; Rare:70 | ||||
| chr5:133026498-133026803 | Common:5; Rare:81 | ||||
| chr5:133051605-133052105 | Common:2; Rare:177 | ||||
| chr5:133967926-133968326 | Common:2; Rare:105 | ||||
| chr5:133968573-133968917 | Common:1; Rare:105 | ||||
| chr5:134004705-134004926 | Common:1; Rare:83 | ||||
| chr5:134114532-134114681 | Rare:48 | ||||
| chr5:134175109-134176471 | Common:9; Rare:358 |