| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115544648-115545034 | Common:2; Rare:145 | ||||
| chr5:115626168-115626348 | Common:2; Rare:47 | ||||
| chr5:115816507-115816550 | Rare:7 | ||||
| chr5:115816594-115816666 | Rare:23 | ||||
| chr5:115816834-115816860 | Rare:8 | ||||
| chr5:115841490-115841617 | Common:2; Rare:81 | ||||
| chr5:115841789-115842046 | Common:4; Rare:85 | ||||
| chr5:116084919-116085067 | Common:6; Rare:69 | ||||
| chr5:116085334-116085498 | Rare:54 | ||||
| chr5:116574513-116574591 | Common:2; Rare:18 | ||||
| chr5:116574821-116574979 | Common:2; Rare:52 | ||||
| chr5:119070838-119071202 | Common:4; Rare:112 | ||||
| chr5:119071356-119071504 | Rare:64 | ||||
| chr5:119268563-119268837 | Common:1; Rare:76 | ||||
| chr5:119452356-119452604 | Common:1; Rare:93; Clinvar:3; Clinvar (benign):4 |