| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139273832-139274132 | Common:1; Rare:123; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:139439453-139439623 | Common:2; Rare:46 | ||||
| chr5:139561137-139561409 | Common:1; Rare:112 | ||||
| chr5:139561723-139561800 | Rare:35 | ||||
| chr5:140107600-140107849 | Rare:91 | ||||
| chr5:140303072-140303363 | Common:1; Rare:83 | ||||
| chr5:140346597-140346721 | Common:1; Rare:34 | ||||
| chr5:140557405-140557519 | Rare:71 | ||||
| chr5:140564296-140564509 | Common:1; Rare:56 | ||||
| chr5:140564556-140564845 | Rare:76 | ||||
| chr5:140639288-140639478 | Common:3; Rare:48 | ||||
| chr5:140647585-140647924 | Common:5; Rare:139; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691317-140691657 | Common:1; Rare:121; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:141245273-141245412 | Rare:31 | ||||
| chr5:141320725-141320928 | Common:3; Rare:71 |