| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134648720-134648885 | Rare:45 | ||||
| chr5:134738426-134738623 | Rare:76 | ||||
| chr5:135034549-135034552 | |||||
| chr5:135363049-135363073 | Rare:4 | ||||
| chr5:135370036-135370358 | Common:1; Rare:62 | ||||
| chr5:135399138-135399429 | Rare:72 | ||||
| chr5:135578987-135579178 | Common:2; Rare:52 | ||||
| chr5:137753891-137754078 | Rare:37 | ||||
| chr5:137880346-137880660 | Common:1; Rare:50 | ||||
| chr5:138033004-138033193 | Common:1; Rare:70 | ||||
| chr5:138338251-138338283 | Common:1; Rare:16 | ||||
| chr5:138543095-138543490 | Common:2; Rare:117 | ||||
| chr5:138557403-138557584 | Rare:47 | ||||
| chr5:138753268-138753507 | Common:2; Rare:81 | ||||
| chr5:138930302-138930654 | Common:1; Rare:72; Clinvar (benign):1 |