| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:76952833-76953121 | Rare:42 | ||||
| chr5:77030284-77030421 | Rare:44 | ||||
| chr5:77086524-77086761 | Common:1; Rare:47 | ||||
| chr5:77087201-77087463 | Rare:43 | ||||
| chr5:78360346-78360683 | Common:5; Rare:130 | ||||
| chr5:79069575-79069806 | Rare:77; Clinvar (benign):2 | ||||
| chr5:79111576-79111918 | Rare:91 | ||||
| chr5:79236012-79236128 | Common:1; Rare:46 | ||||
| chr5:79612264-79612582 | Rare:79 | ||||
| chr5:79689720-79689881 | Common:1; Rare:44 | ||||
| chr5:79991082-79991363 | Rare:97 | ||||
| chr5:80256044-80256257 | Common:1; Rare:86 | ||||
| chr5:80407872-80408103 | Common:1; Rare:83 | ||||
| chr5:80487910-80488126 | Common:1; Rare:69 | ||||
| chr5:80654521-80654700 | Common:5; Rare:104 |