| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:77086967-77087041 | Common:1; Rare:12 | ||||
| chr5:77087172-77087293 | Rare:32 | ||||
| chr5:77087313-77087388 | Rare:7 | ||||
| chr5:77776216-77776542 | Common:2; Rare:119 | ||||
| chr5:78294608-78294842 | Common:1; Rare:92; Clinvar:1 | ||||
| chr5:78360346-78360683 | Common:5; Rare:130 | ||||
| chr5:78648509-78648674 | Common:3; Rare:43 | ||||
| chr5:78648710-78648978 | Common:2; Rare:92 | ||||
| chr5:79069575-79069803 | Rare:76; Clinvar (benign):2 | ||||
| chr5:79235945-79236135 | Common:2; Rare:79 | ||||
| chr5:79513127-79513419 | Rare:68 | ||||
| chr5:79514533-79514689 | Rare:46 | ||||
| chr5:79612267-79612615 | Rare:93 | ||||
| chr5:79991082-79991365 | Rare:97 | ||||
| chr5:80255977-80256277 | Common:2; Rare:115 |