| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:185498932-185499149 | Rare:81 | ||||
| chr3:185821099-185821155 | Rare:12 | ||||
| chr3:185824940-185825183 | Rare:68 | ||||
| chr3:186567286-186567447 | Common:3; Rare:42 | ||||
| chr3:186783253-186783682 | Common:1; Rare:198 | ||||
| chr3:186806295-186806577 | Rare:81 | ||||
| chr3:186930445-186930562 | Rare:39 | ||||
| chr3:187139433-187139564 | Rare:49 | ||||
| chr3:188153750-188153938 | Common:1; Rare:36 | ||||
| chr3:188154055-188154235 | Rare:61 | ||||
| chr3:190120815-190121059 | Rare:72 | ||||
| chr3:190513959-190514128 | Rare:45 | ||||
| chr3:191329245-191329466 | Common:2; Rare:72 | ||||
| chr3:192917652-192918016 | Common:2; Rare:152 | ||||
| chr3:193593090-193593404 | Rare:97; Clinvar:2; Clinvar (benign):2 |