| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:56952310-56952810 | Common:7; Rare:228 | ||||
| chr5:57173490-57174312 | Common:7; Rare:475 | ||||
| chr5:58460028-58460264 | Common:10; Rare:178 | ||||
| chr5:59275360-59276174 | Common:10; Rare:238 | ||||
| chr5:59276175-59276310 | Rare:30 | ||||
| chr5:59767940-59768093 | Rare:27 | ||||
| chr5:59768045-59768212 | Rare:32 | ||||
| chr5:59768433-59768916 | Rare:214 | ||||
| chr5:59768984-59769142 | Common:1; Rare:21 | ||||
| chr5:60700062-60700249 | Common:2; Rare:133 | ||||
| chr5:60844151-60844429 | Common:9; Rare:169 | ||||
| chr5:60944997-60945394 | Common:11; Rare:245; Clinvar:10; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr5:61161890-61162190 | Rare:80 | ||||
| chr5:61162275-61162708 | Common:2; Rare:168 | ||||
| chr5:61331981-61332276 | Rare:200 |