| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:74685053-74685368 | Common:3; Rare:107; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:74767047-74767362 | Common:3; Rare:101 | ||||
| chr5:75511614-75511913 | Common:1; Rare:111 | ||||
| chr5:75717390-75717663 | Common:5; Rare:67 | ||||
| chr5:76715804-76716169 | Common:6; Rare:102 | ||||
| chr5:77087201-77087303 | Rare:25 | ||||
| chr5:78360363-78360677 | Common:5; Rare:122 | ||||
| chr5:79069627-79069784 | Rare:55; Clinvar (benign):2 | ||||
| chr5:79612259-79612500 | Rare:61 | ||||
| chr5:79689774-79690048 | Common:3; Rare:85 | ||||
| chr5:79991208-79991356 | Rare:45 | ||||
| chr5:80256018-80256243 | Common:1; Rare:91 | ||||
| chr5:80487944-80488118 | Common:1; Rare:60 | ||||
| chr5:80654550-80654694 | Common:5; Rare:88 | ||||
| chr5:81233137-81233377 | Common:1; Rare:60 |