| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:56952095-56952464 | Rare:128 | ||||
| chr5:57173569-57173907 | Common:2; Rare:119 | ||||
| chr5:57173918-57174227 | Rare:92 | ||||
| chr5:57245152-57245449 | Common:1; Rare:66 | ||||
| chr5:57482804-57482984 | Rare:34 | ||||
| chr5:58454793-58454991 | Rare:47 | ||||
| chr5:58455463-58455604 | Rare:33 | ||||
| chr5:58456931-58457201 | Common:1; Rare:66 | ||||
| chr5:58458558-58459110 | Common:3; Rare:104 | ||||
| chr5:58459234-58459370 | Common:1; Rare:26 | ||||
| chr5:58459676-58459790 | Rare:37 | ||||
| chr5:58459801-58460008 | Common:1; Rare:74 | ||||
| chr5:60944933-60945416 | Common:7; Rare:193; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr5:61162218-61162508 | Common:1; Rare:61 | ||||
| chr5:61332564-61332942 | Common:5; Rare:122; Clinvar:2 |