| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:51844104-51844373 | Rare:69 | ||||
| chr4:56490341-56490595 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):3 | ||||
| chr4:56490643-56490917 | Common:2; Rare:57 | ||||
| chr4:57008693-57008967 | Common:2; Rare:48 | ||||
| chr4:57103739-57103820 | Rare:9 | ||||
| chr4:66565310-66565560 | Common:1; Rare:53 | ||||
| chr4:68337316-68337682 | Common:1; Rare:115 | ||||
| chr4:70689388-70689492 | Rare:22 | ||||
| chr4:70832182-70832448 | Common:1; Rare:94 | ||||
| chr4:73118691-73118979 | Rare:59 | ||||
| chr4:74370936-74371155 | Common:4; Rare:46 | ||||
| chr4:74452482-74452581 | Rare:21 | ||||
| chr4:77047000-77047183 | Common:1; Rare:31 | ||||
| chr4:77820253-77820608 | Rare:120 | ||||
| chr4:82360340-82360609 | Common:3; Rare:53 |