| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:174441120-174441360 | Common:2; Rare:70 | ||||
| chr3:177196340-177196740 | Common:1; Rare:121 | ||||
| chr3:177197222-177197474 | Rare:81 | ||||
| chr3:177197760-177197980 | Common:1; Rare:75 | ||||
| chr3:178536033-178536396 | Common:7; Rare:82 | ||||
| chr3:179071773-179071896 | Rare:27 | ||||
| chr3:179147952-179148159 | Common:2; Rare:53 | ||||
| chr3:179148356-179148892 | Common:10; Rare:265; Clinvar (benign):2 | ||||
| chr3:179148830-179149375 | Common:1; Rare:203 | ||||
| chr3:179322744-179323088 | Common:6; Rare:103 | ||||
| chr3:179323374-179323539 | Common:1; Rare:47 | ||||
| chr3:179347570-179347807 | Common:1; Rare:60 | ||||
| chr3:179451391-179451728 | Common:2; Rare:117 | ||||
| chr3:179562584-179563055 | Rare:153 | ||||
| chr3:179563186-179563338 | Rare:44 |