| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134411850-134411990 | Rare:45 | ||||
| chr5:134632773-134632937 | Rare:32 | ||||
| chr5:134648688-134648848 | Rare:48 | ||||
| chr5:134738418-134738615 | Rare:75 | ||||
| chr5:134758615-134758804 | Common:1; Rare:56 | ||||
| chr5:134845824-134846121 | Rare:133 | ||||
| chr5:134874236-134874423 | Common:1; Rare:90 | ||||
| chr5:136132751-136132944 | Common:1; Rare:59 | ||||
| chr5:137889312-137889484 | Common:1; Rare:68 | ||||
| chr5:138033047-138033137 | Common:1; Rare:36 | ||||
| chr5:138543095-138543513 | Common:2; Rare:128 | ||||
| chr5:138753301-138753488 | Common:2; Rare:59 | ||||
| chr5:138875197-138875478 | Common:1; Rare:52; Clinvar (benign):1 | ||||
| chr5:139198289-139198579 | Common:1; Rare:98; Clinvar (benign):1 | ||||
| chr5:139293575-139293809 | Rare:76 |