| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:176002330-176002713 | Rare:102 | ||||
| chr4:176319850-176320028 | Common:2; Rare:74 | ||||
| chr4:177309778-177309870 | Common:1; Rare:27 | ||||
| chr4:177442371-177442521 | Rare:90; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182917325-182917551 | Common:4; Rare:78 | ||||
| chr4:183444301-183444697 | Common:2; Rare:168 | ||||
| chr4:183504522-183504809 | Common:2; Rare:94 | ||||
| chr4:183506060-183506095 | Rare:10 | ||||
| chr4:183659096-183659417 | Common:1; Rare:106 | ||||
| chr4:184474524-184474808 | Rare:65 | ||||
| chr4:184649399-184649796 | Common:4; Rare:130 | ||||
| chr4:184734041-184734365 | Common:5; Rare:128 | ||||
| chr4:185203884-185204097 | Rare:69 | ||||
| chr4:185396556-185396851 | Rare:96 | ||||
| chr4:185425880-185426272 | Common:4; Rare:116 |