| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32217648-32217704 | Common:1; Rare:9 | ||||
| chr13:32225660-32226005 | Rare:83 | ||||
| chr13:32228440-32228697 | Rare:79 | ||||
| chr13:32246624-32246671 | Rare:7 | ||||
| chr13:32255789-32256023 | Common:1; Rare:48 | ||||
| chr13:32261032-32261231 | Common:2; Rare:27 | ||||
| chr13:32427091-32427225 | Common:2; Rare:26 | ||||
| chr13:32438992-32439142 | Common:2; Rare:23 | ||||
| chr13:32475419-32475643 | Rare:45 | ||||
| chr13:32587253-32587335 | Common:2; Rare:22 | ||||
| chr13:32587628-32587670 | Rare:11 | ||||
| chr13:32824748-32825016 | Common:1; Rare:54 | ||||
| chr13:33017015-33017117 | Rare:36; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr13:33017591-33017774 | Rare:33 | ||||
| chr13:33125877-33126107 | Common:1; Rare:52 |