| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48779632-48779824 | Rare:65 | ||||
| chr4:48780175-48780663 | Common:4; Rare:156 | ||||
| chr4:48830821-48831250 | Common:1; Rare:133 | ||||
| chr4:48831320-48831375 | Rare:9 | ||||
| chr4:48831749-48831846 | Rare:18 | ||||
| chr4:48906687-48906916 | Rare:52 | ||||
| chr4:51842730-51843292 | Common:2; Rare:165 | ||||
| chr4:51844637-51844928 | Common:1; Rare:89 | ||||
| chr4:52038240-52038431 | Rare:72; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52051967-52052070 | Rare:24 | ||||
| chr4:52658968-52659003 | Common:1; Rare:9 | ||||
| chr4:52659161-52659495 | Common:1; Rare:111 | ||||
| chr4:52862165-52862343 | Common:8; Rare:78 | ||||
| chr4:53365916-53366327 | Common:2; Rare:100 | ||||
| chr4:53377427-53377699 | Common:3; Rare:80 |