| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:24537148-24537274 | Rare:19 | ||||
| chr4:25657034-25657338 | Rare:57 | ||||
| chr4:25671586-25671800 | Common:2; Rare:64 | ||||
| chr4:25674276-25674629 | Common:3; Rare:120 | ||||
| chr4:26275383-26275497 | Rare:22 | ||||
| chr4:37615636-37615893 | Common:2; Rare:44 | ||||
| chr4:38664855-38665051 | Rare:54 | ||||
| chr4:40816202-40816451 | Common:1; Rare:45 | ||||
| chr4:41050939-41051186 | Common:2; Rare:58 | ||||
| chr4:54232873-54233142 | Common:5; Rare:69 | ||||
| chr4:54288813-54289108 | Rare:71; Clinvar:9; Clinvar (benign):6 | ||||
| chr4:55890021-55890341 | Common:1; Rare:70 | ||||
| chr4:55947867-55948228 | Common:2; Rare:64 | ||||
| chr4:56486143-56486395 | Common:1; Rare:52 | ||||
| chr4:56976924-56976999 | Common:1; Rare:25 |