| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140107679-140107846 | Rare:57 | ||||
| chr5:140175002-140175253 | Rare:69 | ||||
| chr5:140557427-140557540 | Common:1; Rare:69 | ||||
| chr5:140564273-140564553 | Common:2; Rare:71 | ||||
| chr5:140564573-140564837 | Rare:73 | ||||
| chr5:140639131-140639478 | Common:4; Rare:78 | ||||
| chr5:140647559-140647903 | Common:5; Rare:141; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691317-140691648 | Common:1; Rare:116; Clinvar:10; Clinvar (benign):1 | ||||
| chr5:141320750-141320928 | Common:2; Rare:59 | ||||
| chr5:141475732-141476021 | Common:2; Rare:58 | ||||
| chr5:141636818-141636968 | Common:1; Rare:62 | ||||
| chr5:141637335-141637452 | Common:1; Rare:26 | ||||
| chr5:141923649-141923910 | Common:1; Rare:79 | ||||
| chr5:142108660-142108970 | Common:3; Rare:109 | ||||
| chr5:142324973-142325183 | Rare:78 |