| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:174283612-174283977 | Common:1; Rare:74 | ||||
| chr4:174522423-174522613 | Rare:62; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:176065729-176066001 | Common:7; Rare:88 | ||||
| chr4:176195566-176195744 | Common:2; Rare:69 | ||||
| chr4:176319742-176320048 | Common:3; Rare:107 | ||||
| chr4:177442376-177442530 | Rare:93; Clinvar:2 | ||||
| chr4:182143907-182143968 | Rare:13 | ||||
| chr4:182448669-182449062 | Common:4; Rare:120 | ||||
| chr4:183099010-183099281 | Common:2; Rare:92 | ||||
| chr4:183504522-183504795 | Common:1; Rare:92 | ||||
| chr4:183505981-183506111 | Rare:53 | ||||
| chr4:183659090-183659417 | Common:1; Rare:107 | ||||
| chr4:184649406-184649796 | Common:4; Rare:126 | ||||
| chr4:184734121-184734430 | Common:6; Rare:92 | ||||
| chr4:184805480-184805813 | Common:1; Rare:63 |