| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147684124-147684302 | Common:1; Rare:75 | ||||
| chr4:150581734-150581974 | Rare:50 | ||||
| chr4:152779799-152780183 | Common:2; Rare:93 | ||||
| chr4:155352947-155353335 | Common:1; Rare:102 | ||||
| chr4:156970916-156971059 | Rare:23 | ||||
| chr4:158172347-158172730 | Rare:62 | ||||
| chr4:158671825-158672358 | Common:5; Rare:135; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:159229190-159229422 | Common:1; Rare:39 | ||||
| chr4:163166829-163166972 | Common:2; Rare:46 | ||||
| chr4:163494623-163494807 | Common:2; Rare:69 | ||||
| chr4:168921261-168921652 | Common:2; Rare:69; Clinvar:2 | ||||
| chr4:169660036-169660293 | Common:1; Rare:46 | ||||
| chr4:173168550-173168841 | Common:2; Rare:88 | ||||
| chr4:173370683-173371012 | Common:2; Rare:84 | ||||
| chr4:173399173-173399531 | Common:10; Rare:60 |