| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:78510316-78510503 | Common:1; Rare:42 | ||||
| chr5:78510520-78510561 | Common:1; Rare:8 | ||||
| chr5:78510570-78510606 | Rare:4 | ||||
| chr5:79547572-79547753 | Common:2; Rare:26 | ||||
| chr5:80650893-80651186 | Common:2; Rare:57 | ||||
| chr5:80778429-80778798 | Rare:109; Clinvar (pathogenic):1 | ||||
| chr5:87362351-87362641 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:87366129-87366353 | Common:1; Rare:46 | ||||
| chr5:87383846-87384109 | Rare:45 | ||||
| chr5:87393123-87393148 | Common:1; Rare:4 | ||||
| chr5:93580666-93580919 | Common:1; Rare:61 | ||||
| chr5:95816057-95816372 | Common:1; Rare:45 | ||||
| chr5:96765857-96766134 | Rare:46 | ||||
| chr5:96770372-96770576 | Common:1; Rare:40 | ||||
| chr5:96778141-96778264 | Rare:17 |