| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56387414-56387543 | Rare:42 | ||||
| chr4:56435481-56435973 | Common:6; Rare:161 | ||||
| chr4:56436037-56436315 | Rare:103 | ||||
| chr4:56467422-56467684 | Common:2; Rare:98; Clinvar (benign):4 | ||||
| chr4:56681287-56681523 | Common:1; Rare:35 | ||||
| chr4:56977592-56977765 | Common:1; Rare:62 | ||||
| chr4:57109877-57110159 | Rare:98 | ||||
| chr4:57110365-57110530 | Common:1; Rare:55 | ||||
| chr4:67545433-67545743 | Common:2; Rare:78 | ||||
| chr4:67701099-67701358 | Common:4; Rare:125 | ||||
| chr4:68349734-68349796 | Rare:32 | ||||
| chr4:68349861-68350228 | Common:2; Rare:119 | ||||
| chr4:69050992-69051230 | Rare:55 | ||||
| chr4:70688345-70688586 | Common:2; Rare:61 | ||||
| chr4:70902206-70902378 | Common:4; Rare:65 |