| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173168743-173168844 | Common:2; Rare:43 | ||||
| chr4:173333498-173333867 | Common:2; Rare:94 | ||||
| chr4:173334280-173334769 | Rare:126 | ||||
| chr4:173369784-173369971 | Common:1; Rare:62 | ||||
| chr4:173370674-173370982 | Common:2; Rare:79 | ||||
| chr4:174283601-174284046 | Common:1; Rare:97 | ||||
| chr4:174284262-174284376 | Common:1; Rare:27 | ||||
| chr4:174522449-174522592 | Rare:46; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:175812198-175812368 | Common:11; Rare:54 | ||||
| chr4:175812375-175812536 | Rare:32 | ||||
| chr4:175812767-175812848 | Rare:16 | ||||
| chr4:176065737-176066040 | Common:7; Rare:96 | ||||
| chr4:176195583-176195722 | Common:1; Rare:51 | ||||
| chr4:176319713-176320149 | Common:5; Rare:133 | ||||
| chr4:177309759-177309944 | Common:2; Rare:56 |