| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:28495280-28495616 | Common:3; Rare:73 | ||||
| chr13:28658948-28659210 | Common:1; Rare:113; Clinvar (pathogenic):1 | ||||
| chr13:28718787-28719123 | Common:1; Rare:86 | ||||
| chr13:29850566-29850671 | Common:1; Rare:58 | ||||
| chr13:30306832-30307197 | Common:6; Rare:98 | ||||
| chr13:30307368-30307596 | Common:2; Rare:77 | ||||
| chr13:30465760-30466134 | Common:1; Rare:115 | ||||
| chr13:30616972-30617171 | Rare:39 | ||||
| chr13:30617263-30617418 | Rare:37 | ||||
| chr13:30617579-30618047 | Common:1; Rare:142 | ||||
| chr13:32315342-32315538 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:32586248-32586582 | Common:2; Rare:101 | ||||
| chr13:33206022-33206124 | Rare:24 | ||||
| chr13:33285670-33285897 | Rare:51 | ||||
| chr13:33818045-33818217 | Rare:82 |