| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:53480288-53480527 | Common:2; Rare:48 | ||||
| chr5:53560616-53560726 | Common:2; Rare:116; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:54310434-54310741 | Common:3; Rare:171 | ||||
| chr5:55160091-55160193 | Rare:22 | ||||
| chr5:55173060-55173430 | Common:3; Rare:162 | ||||
| chr5:55227140-55227580 | Common:2; Rare:147 | ||||
| chr5:55233584-55233922 | Common:11; Rare:222 | ||||
| chr5:55307608-55308069 | Common:9; Rare:302 | ||||
| chr5:55322130-55322670 | Common:1; Rare:168 | ||||
| chr5:55534949-55535183 | Common:2; Rare:156 | ||||
| chr5:55994794-55995374 | Rare:312 | ||||
| chr5:56815212-56815589 | Common:5; Rare:250 | ||||
| chr5:56909050-56909710 | Common:4; Rare:221 | ||||
| chr5:56909764-56909955 | Common:6; Rare:80 | ||||
| chr5:56952082-56952265 | Rare:87 |