| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167734799-167735237 | Common:3; Rare:144; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735609-167735752 | Rare:35 | ||||
| chr3:168044857-168045168 | Common:1; Rare:58 | ||||
| chr3:169147302-169147495 | Common:2; Rare:45 | ||||
| chr3:169773341-169773424 | Rare:25 | ||||
| chr3:169812514-169812758 | Common:2; Rare:61 | ||||
| chr3:169966667-169967088 | Common:5; Rare:140 | ||||
| chr3:169982426-169982807 | Common:4; Rare:87 | ||||
| chr3:170037940-170038204 | Common:5; Rare:68 | ||||
| chr3:170870163-170870312 | Rare:76 | ||||
| chr3:170908590-170908839 | Common:1; Rare:70 | ||||
| chr3:171460150-171460499 | Common:2; Rare:80 | ||||
| chr3:172039494-172039657 | Common:1; Rare:52 | ||||
| chr3:172522892-172523181 | Rare:54 | ||||
| chr3:172523244-172523316 | Common:1; Rare:23 |