| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197950645-197950978 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197960013-197960242 | Common:1; Rare:83 | ||||
| chr4:337477-337873 | Common:2; Rare:117 | ||||
| chr4:499132-499281 | Common:3; Rare:50 | ||||
| chr4:663642-663737 | Rare:29 | ||||
| chr4:674212-674585 | Common:4; Rare:171 | ||||
| chr4:932250-932487 | Common:2; Rare:93 | ||||
| chr4:986930-987175 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113512-1113630 | Common:2; Rare:41 | ||||
| chr4:1172821-1173148 | Common:5; Rare:48 | ||||
| chr4:1346970-1347210 | Common:4; Rare:69 | ||||
| chr4:1720296-1720596 | Common:3; Rare:80 | ||||
| chr4:2468888-2469200 | Common:4; Rare:131 | ||||
| chr4:2843710-2844018 | Common:3; Rare:109 | ||||
| chr4:2934767-2934910 | Common:1; Rare:66 |