| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:78758407-78758709 | Common:1; Rare:46 | ||||
| chr5:78760575-78760719 | Rare:22 | ||||
| chr5:78984093-78984187 | Common:1; Rare:20 | ||||
| chr5:78984532-78985051 | Common:10; Rare:189; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr5:79237006-79237116 | Rare:50 | ||||
| chr5:79237343-79237570 | Rare:75 | ||||
| chr5:79237603-79237797 | Common:1; Rare:45 | ||||
| chr5:79561236-79561440 | Rare:33 | ||||
| chr5:80247382-80247516 | Common:1; Rare:24 | ||||
| chr5:80256810-80256857 | Rare:11 | ||||
| chr5:80407060-80407178 | Rare:18 | ||||
| chr5:80607994-80608137 | Common:1; Rare:17 | ||||
| chr5:80668141-80668359 | Common:1; Rare:53 | ||||
| chr5:80755781-80755931 | Rare:26 | ||||
| chr5:81187948-81188076 | Common:2; Rare:21 |