| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179604630-179604852 | Common:2; Rare:78 | ||||
| chr3:180602127-180602242 | Common:1; Rare:42 | ||||
| chr3:180989652-180989790 | Rare:60; Clinvar:1 | ||||
| chr3:181711718-181711971 | Rare:79 | ||||
| chr3:183099443-183099755 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183253056-183253288 | Common:3; Rare:71 | ||||
| chr3:184017876-184017999 | Rare:30 | ||||
| chr3:184135219-184135391 | Common:2; Rare:51; Clinvar:5 | ||||
| chr3:184185925-184186203 | Common:4; Rare:106 | ||||
| chr3:184298947-184299269 | Common:3; Rare:99 | ||||
| chr3:184314428-184314671 | Common:3; Rare:72 | ||||
| chr3:184711864-184712260 | Common:2; Rare:131 | ||||
| chr3:185282868-185283006 | Common:1; Rare:37 | ||||
| chr3:185498968-185499155 | Rare:66 | ||||
| chr3:186567291-186567403 | Common:3; Rare:31 |