| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:163662910-163663088 | Common:3; Rare:37 | ||||
| chr4:168903618-168903905 | Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:168924685-168925068 | Common:2; Rare:88; Clinvar:3; Clinvar (benign):3 | ||||
| chr4:173416187-173416299 | Common:2; Rare:19 | ||||
| chr4:173509555-173509676 | Common:1; Rare:34 | ||||
| chr4:175771165-175771273 | Common:3; Rare:13 | ||||
| chr4:176320515-176320612 | Rare:30 | ||||
| chr4:183806526-183806547 | Rare:5 | ||||
| chr4:184265760-184265784 | Rare:2 | ||||
| chr4:184265795-184266167 | Rare:50 | ||||
| chr4:184266210-184266383 | Rare:34 | ||||
| chr4:184280705-184280956 | Rare:41 | ||||
| chr4:184382232-184382478 | Common:4; Rare:39 | ||||
| chr4:184392940-184393222 | Common:2; Rare:57 | ||||
| chr4:184432405-184432713 | Common:3; Rare:58 |