| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:126423354-126423625 | Rare:81 | ||||
| chr5:127030509-127030707 | Common:2; Rare:48 | ||||
| chr5:127517516-127517699 | Common:4; Rare:79 | ||||
| chr5:131170704-131171018 | Common:1; Rare:64; Clinvar (benign):2 | ||||
| chr5:131635160-131635416 | Common:1; Rare:98 | ||||
| chr5:131796926-131797215 | Rare:84 | ||||
| chr5:132369604-132369977 | Common:7; Rare:123; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:132490750-132491020 | Rare:70 | ||||
| chr5:132830619-132830775 | Rare:44 | ||||
| chr5:132866435-132866698 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963581-132963782 | Rare:56 | ||||
| chr5:133051887-133052354 | Common:1; Rare:144 | ||||
| chr5:133968554-133968722 | Rare:68 | ||||
| chr5:134004515-134004843 | Common:2; Rare:112 | ||||
| chr5:134004894-134005082 | Rare:40 |