| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:44918002-44918128 | Common:2; Rare:66 | ||||
| chr13:48580931-48581135 | Common:1; Rare:35 | ||||
| chr13:52194379-52194537 | Rare:45 | ||||
| chr13:52617393-52617541 | Common:1; Rare:36 | ||||
| chr13:76885086-76885348 | Rare:94 | ||||
| chr13:76885482-76885798 | Common:1; Rare:116 | ||||
| chr13:87671268-87671392 | Rare:38 | ||||
| chr13:93227543-93227615 | Rare:37 | ||||
| chr13:93228222-93228285 | Common:1; Rare:17 | ||||
| chr13:95790695-95790876 | Rare:32 | ||||
| chr13:97223797-97224108 | Common:2; Rare:66 | ||||
| chr13:99296073-99296360 | Rare:74 | ||||
| chr13:102394500-102394646 | Common:1; Rare:54 | ||||
| chr13:110192818-110192969 | Common:2; Rare:46; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr13:110281239-110281436 | Common:2; Rare:29 |