| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149812564-149812777 | Common:1; Rare:59 | ||||
| chr3:149812992-149813313 | Common:2; Rare:106 | ||||
| chr3:149814151-149814312 | Common:1; Rare:26 | ||||
| chr3:149970723-149971006 | Rare:102 | ||||
| chr3:149971126-149971349 | Common:3; Rare:104 | ||||
| chr3:150050685-150050835 | Common:2; Rare:55 | ||||
| chr3:150408169-150408377 | Common:2; Rare:87 | ||||
| chr3:150603145-150603367 | Common:2; Rare:86 | ||||
| chr3:150703423-150703518 | Rare:28 | ||||
| chr3:150703894-150704025 | Rare:49 | ||||
| chr3:151085569-151085828 | Rare:100 | ||||
| chr3:151086470-151086718 | Common:5; Rare:63 | ||||
| chr3:152268439-152268642 | Common:2; Rare:59; Clinvar (benign):1 | ||||
| chr3:152268839-152269213 | Rare:121 | ||||
| chr3:152269220-152269342 | Rare:37 |