| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:72727598-72727962 | Common:4; Rare:138 | ||||
| chr13:72781859-72782198 | Common:1; Rare:133 | ||||
| chr13:75549363-75549817 | Common:8; Rare:118 | ||||
| chr13:76991943-76992181 | Common:3; Rare:115; Clinvar:21; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr13:77027142-77027289 | Common:5; Rare:43 | ||||
| chr13:79405797-79405882 | Rare:31 | ||||
| chr13:79406253-79406320 | Common:1; Rare:23 | ||||
| chr13:79481034-79481378 | Common:2; Rare:138 | ||||
| chr13:94596126-94596325 | Common:2; Rare:69 | ||||
| chr13:94601592-94601918 | Common:3; Rare:94 | ||||
| chr13:95676933-95677177 | Common:3; Rare:80 | ||||
| chr13:96053360-96053490 | Common:2; Rare:49 | ||||
| chr13:99200663-99200900 | Common:6; Rare:110 | ||||
| chr13:102596785-102597048 | Common:1; Rare:125; Clinvar (benign):1 | ||||
| chr13:102773766-102773860 | Rare:37 |