| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43313360-43313674 | Common:3; Rare:83 | ||||
| chr5:43483837-43483970 | Common:1; Rare:46 | ||||
| chr5:43515133-43515259 | Common:2; Rare:46 | ||||
| chr5:43602592-43602746 | Common:2; Rare:29 | ||||
| chr5:43602886-43603293 | Rare:99 | ||||
| chr5:44808722-44808999 | Common:2; Rare:103 | ||||
| chr5:44809341-44809407 | Common:1; Rare:30 | ||||
| chr5:44809409-44809484 | Rare:38 | ||||
| chr5:50665663-50665922 | Common:1; Rare:34 | ||||
| chr5:50667107-50667411 | Common:1; Rare:97 | ||||
| chr5:50667473-50667570 | Rare:31 | ||||
| chr5:50667779-50667957 | Common:1; Rare:57 | ||||
| chr5:52787823-52787971 | Common:1; Rare:28 | ||||
| chr5:52788023-52788370 | Common:1; Rare:85 | ||||
| chr5:53109711-53109977 | Common:1; Rare:121; Clinvar:4; Clinvar (pathogenic):1 |