| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139561975-139562375 | Common:2; Rare:272 | ||||
| chr5:139648174-139648428 | Common:1; Rare:74 | ||||
| chr5:139648760-139648974 | Rare:60 | ||||
| chr5:140107726-140107828 | Rare:28 | ||||
| chr5:140113987-140114185 | Rare:51 | ||||
| chr5:140174919-140175217 | Rare:94 | ||||
| chr5:140303028-140303255 | Common:1; Rare:74 | ||||
| chr5:140346589-140346898 | Common:1; Rare:80 | ||||
| chr5:140401391-140401844 | Common:3; Rare:89 | ||||
| chr5:140557397-140557619 | Common:3; Rare:115 | ||||
| chr5:140564573-140564862 | Rare:78 | ||||
| chr5:140639270-140639528 | Common:3; Rare:65 | ||||
| chr5:140647561-140647886 | Common:5; Rare:133; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664680-140664910 | Common:4; Rare:56 | ||||
| chr5:140691280-140691504 | Common:2; Rare:88; Clinvar:9; Clinvar (benign):1 |