| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:55546567-55546706 | Common:2; Rare:26 | ||||
| chr4:55546801-55547012 | Common:2; Rare:73 | ||||
| chr4:55547102-55547161 | Rare:20 | ||||
| chr4:55592097-55592342 | Common:6; Rare:65 | ||||
| chr4:55636162-55636394 | Common:1; Rare:69 | ||||
| chr4:55853469-55853822 | Rare:104 | ||||
| chr4:55948701-55949006 | Common:2; Rare:66 | ||||
| chr4:56246417-56246526 | Rare:21 | ||||
| chr4:56308723-56308981 | Rare:37 | ||||
| chr4:56387409-56387553 | Rare:48 | ||||
| chr4:56435439-56436327 | Common:6; Rare:298 | ||||
| chr4:56467515-56467931 | Common:3; Rare:153; Clinvar (benign):5 | ||||
| chr4:56505647-56505850 | Common:2; Rare:51 | ||||
| chr4:56530421-56530636 | Common:4; Rare:54 | ||||
| chr4:56557603-56557754 | Common:2; Rare:26 |