| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131994541-131994742 | Common:1; Rare:33 | ||||
| chr5:132294111-132294468 | Common:1; Rare:82 | ||||
| chr5:132295320-132295454 | Rare:29 | ||||
| chr5:132369579-132369785 | Common:4; Rare:63; Clinvar (benign):1 | ||||
| chr5:132410822-132410951 | Rare:24 | ||||
| chr5:132490750-132491020 | Rare:70 | ||||
| chr5:132556777-132557072 | Common:1; Rare:97; Clinvar:1 | ||||
| chr5:132737479-132737650 | Rare:56 | ||||
| chr5:132830610-132830897 | Common:1; Rare:79 | ||||
| chr5:132866415-132866716 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963503-132963737 | Rare:62 | ||||
| chr5:133026504-133026825 | Common:5; Rare:86 | ||||
| chr5:133051843-133052216 | Rare:128 | ||||
| chr5:133968542-133968703 | Rare:73 | ||||
| chr5:134004516-134004906 | Common:2; Rare:135 |