| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127517490-127517757 | Common:7; Rare:112 | ||||
| chr5:129094470-129094769 | Common:3; Rare:123 | ||||
| chr5:131170670-131171002 | Common:1; Rare:75; Clinvar (benign):1 | ||||
| chr5:131635177-131635446 | Common:1; Rare:102 | ||||
| chr5:131796969-131797215 | Rare:67 | ||||
| chr5:132227304-132227466 | Common:1; Rare:34 | ||||
| chr5:132227789-132228195 | Common:4; Rare:100 | ||||
| chr5:132490774-132491055 | Rare:72 | ||||
| chr5:132556836-132556997 | Common:1; Rare:56; Clinvar:1 | ||||
| chr5:132866387-132866698 | Common:1; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963603-132963834 | Common:1; Rare:60 | ||||
| chr5:133051851-133052216 | Rare:125 | ||||
| chr5:133968554-133968737 | Rare:73 | ||||
| chr5:134004516-134004877 | Common:2; Rare:125 | ||||
| chr5:134004905-134005074 | Rare:34 |