| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:176320089-176320215 | Rare:22 | ||||
| chr4:177309750-177309948 | Common:2; Rare:63 | ||||
| chr4:177442359-177442554 | Rare:116; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182143807-182144057 | Common:2; Rare:56 | ||||
| chr4:182144170-182144232 | Common:5; Rare:23 | ||||
| chr4:182144408-182144743 | Common:3; Rare:114 | ||||
| chr4:182448789-182449081 | Common:2; Rare:103 | ||||
| chr4:183099039-183099306 | Common:2; Rare:87 | ||||
| chr4:183444426-183444754 | Common:2; Rare:154 | ||||
| chr4:183504377-183504893 | Common:3; Rare:164 | ||||
| chr4:183659160-183659407 | Common:1; Rare:80 | ||||
| chr4:184474490-184474765 | Rare:63 | ||||
| chr4:184649375-184649805 | Common:5; Rare:141 | ||||
| chr4:184733350-184733530 | Common:4; Rare:50 | ||||
| chr4:184734014-184734467 | Common:11; Rare:182 |