| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35176061-35176244 | Common:1; Rare:49 | ||||
| chr20:35176526-35176857 | Common:2; Rare:91 | ||||
| chr20:35277627-35278187 | Common:8; Rare:184 | ||||
| chr20:35284486-35284817 | Common:3; Rare:99 | ||||
| chr20:35473208-35473535 | Rare:87 | ||||
| chr20:35473675-35473971 | Common:1; Rare:60 | ||||
| chr20:35542193-35542949 | Common:1; Rare:235 | ||||
| chr20:35554721-35555073 | Common:4; Rare:68 | ||||
| chr20:35555734-35556269 | Common:2; Rare:143 | ||||
| chr20:35556705-35557284 | Common:2; Rare:166 | ||||
| chr20:35631499-35631731 | Common:3; Rare:78 | ||||
| chr20:35664867-35665043 | Common:1; Rare:47 | ||||
| chr20:35699305-35699647 | Rare:109; Clinvar (benign):3 | ||||
| chr20:35740807-35741167 | Common:3; Rare:97 | ||||
| chr20:35741599-35741693 | Common:1; Rare:30 |