| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:14143093-14143550 | Rare:216 | ||||
| chr5:14664569-14664810 | Common:6; Rare:188 | ||||
| chr5:14871594-14872074 | Common:4; Rare:205; Clinvar (benign):2 | ||||
| chr5:16465680-16465944 | Common:2; Rare:115 | ||||
| chr5:16738110-16738700 | Common:12; Rare:172 | ||||
| chr5:16758300-16758700 | Common:1; Rare:80 | ||||
| chr5:16936234-16936480 | Common:3; Rare:73 | ||||
| chr5:31532021-31532458 | Common:10; Rare:243 | ||||
| chr5:32173440-32174180 | Common:1; Rare:286 | ||||
| chr5:32174182-32174478 | Common:5; Rare:179 | ||||
| chr5:32174647-32174781 | Common:2; Rare:68 | ||||
| chr5:32233710-32234240 | Common:4; Rare:210 | ||||
| chr5:32312839-32313379 | Common:6; Rare:293 | ||||
| chr5:32444611-32444837 | Rare:153 | ||||
| chr5:32531601-32531871 | Common:1; Rare:46 |