| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:74157818-74158188 | Common:2; Rare:159 | ||||
| chr4:75514260-75514502 | Common:1; Rare:84 | ||||
| chr4:75514707-75514768 | Rare:13 | ||||
| chr4:75673288-75673692 | Common:1; Rare:158 | ||||
| chr4:75724374-75724769 | Common:2; Rare:114 | ||||
| chr4:75990884-75991066 | Common:1; Rare:73 | ||||
| chr4:76148357-76148594 | Common:4; Rare:73 | ||||
| chr4:76949541-76949901 | Common:2; Rare:121 | ||||
| chr4:77075955-77076105 | Common:3; Rare:82 | ||||
| chr4:77076285-77076397 | Common:3; Rare:55 | ||||
| chr4:77158329-77158404 | Rare:27 | ||||
| chr4:77862632-77862911 | Common:3; Rare:110 | ||||
| chr4:78939310-78939515 | Common:2; Rare:90 | ||||
| chr4:80072617-80072851 | Common:2; Rare:64; Clinvar (benign):2 | ||||
| chr4:80073063-80073191 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):1 |