| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:28658948-28659184 | Rare:103; Clinvar (pathogenic):1 | ||||
| chr13:30307001-30307211 | Common:4; Rare:54 | ||||
| chr13:30307384-30307583 | Common:2; Rare:73 | ||||
| chr13:30617479-30618000 | Common:1; Rare:171 | ||||
| chr13:32315409-32315525 | Common:1; Rare:30; Clinvar:1 | ||||
| chr13:32428116-32428238 | Rare:23 | ||||
| chr13:33206022-33206146 | Rare:25 | ||||
| chr13:33285670-33285969 | Common:1; Rare:66 | ||||
| chr13:35476647-35476741 | Common:1; Rare:12 | ||||
| chr13:36346301-36346454 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:37000532-37000808 | Common:3; Rare:89 | ||||
| chr13:37059600-37059754 | Common:1; Rare:51 | ||||
| chr13:37598615-37598903 | Common:2; Rare:84 | ||||
| chr13:39038107-39038426 | Common:1; Rare:81 | ||||
| chr13:39655633-39655765 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 |