| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:79406202-79406339 | Common:4; Rare:42 | ||||
| chr13:87672912-87673056 | Rare:32 | ||||
| chr13:93226510-93226878 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr13:93226885-93227398 | Common:1; Rare:107; Clinvar:6; Clinvar (benign):1 | ||||
| chr13:94596118-94596334 | Common:2; Rare:75 | ||||
| chr13:94601574-94601948 | Common:4; Rare:121 | ||||
| chr13:95301389-95301580 | Rare:54 | ||||
| chr13:95676828-95677238 | Common:4; Rare:159 | ||||
| chr13:96053321-96053519 | Common:2; Rare:92 | ||||
| chr13:97222106-97222406 | Rare:54 | ||||
| chr13:97976404-97976711 | Common:1; Rare:115 | ||||
| chr13:99200652-99200904 | Common:7; Rare:118 | ||||
| chr13:99606467-99606698 | Common:6; Rare:66 | ||||
| chr13:100088858-100089126 | Rare:102; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100588756-100588866 | Common:2; Rare:29 |