| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134758579-134758820 | Common:1; Rare:82 | ||||
| chr5:134845824-134846124 | Rare:133 | ||||
| chr5:134874282-134874436 | Common:1; Rare:84 | ||||
| chr5:134905100-134905195 | Common:1; Rare:23 | ||||
| chr5:135399090-135399343 | Rare:65 | ||||
| chr5:136132777-136132946 | Common:1; Rare:51 | ||||
| chr5:137754332-137754464 | Rare:38 | ||||
| chr5:138033047-138033175 | Common:1; Rare:47 | ||||
| chr5:138178613-138178679 | Rare:22 | ||||
| chr5:138178923-138179178 | Common:3; Rare:54 | ||||
| chr5:138331753-138332108 | Common:2; Rare:91 | ||||
| chr5:138337982-138338290 | Common:2; Rare:117 | ||||
| chr5:138543095-138543506 | Common:2; Rare:123 | ||||
| chr5:138753255-138753488 | Common:2; Rare:81 | ||||
| chr5:139198284-139198525 | Rare:81; Clinvar (benign):1 |