| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:83034849-83035226 | Common:1; Rare:92 | ||||
| chr4:83455772-83456079 | Common:3; Rare:116 | ||||
| chr4:83485079-83485297 | Common:3; Rare:93 | ||||
| chr4:83536135-83536321 | Rare:52 | ||||
| chr4:84966648-84966755 | Rare:29 | ||||
| chr4:85827649-85827958 | Common:1; Rare:46 | ||||
| chr4:86594044-86594378 | Rare:107 | ||||
| chr4:86934892-86935186 | Common:2; Rare:116 | ||||
| chr4:86936177-86936403 | Common:1; Rare:49 | ||||
| chr4:87422516-87422897 | Common:2; Rare:107 | ||||
| chr4:88379040-88379103 | Common:1; Rare:22 | ||||
| chr4:88592306-88592535 | Common:1; Rare:69 | ||||
| chr4:89111410-89111614 | Common:2; Rare:75 | ||||
| chr4:89836971-89837242 | Common:3; Rare:87; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:94451758-94451995 | Common:3; Rare:84 |