| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:174440903-174441007 | Common:1; Rare:27 | ||||
| chr3:177196367-177196666 | Rare:88 | ||||
| chr3:179147998-179148196 | Common:3; Rare:66 | ||||
| chr3:179347595-179347799 | Common:1; Rare:51 | ||||
| chr3:179604614-179604903 | Common:2; Rare:118 | ||||
| chr3:180602111-180602384 | Common:1; Rare:97 | ||||
| chr3:180912356-180912710 | Common:3; Rare:119 | ||||
| chr3:180989618-180989793 | Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:182793365-182793710 | Common:3; Rare:93 | ||||
| chr3:183253154-183253391 | Common:1; Rare:61 | ||||
| chr3:183635323-183635708 | Common:4; Rare:103 | ||||
| chr3:184017870-184018086 | Common:1; Rare:66 | ||||
| chr3:184135221-184135398 | Common:2; Rare:55; Clinvar:5 | ||||
| chr3:184141995-184142275 | Rare:76; Clinvar:1 | ||||
| chr3:184155299-184155359 | Rare:21 |