| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:54657812-54658000 | Common:2; Rare:73 | ||||
| chr4:55346114-55346369 | Common:3; Rare:84; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55346470-55346770 | Common:2; Rare:101; Clinvar:1 | ||||
| chr4:55395815-55396002 | Common:2; Rare:56; Clinvar:2 | ||||
| chr4:55396323-55396972 | Common:12; Rare:238; Clinvar (benign):1 | ||||
| chr4:55545480-55546120 | Common:4; Rare:152 | ||||
| chr4:55546680-55546808 | Common:3; Rare:40 | ||||
| chr4:55546967-55547318 | Common:7; Rare:230 | ||||
| chr4:55547429-55547617 | Common:1; Rare:34 | ||||
| chr4:55636160-55636610 | Common:2; Rare:105 | ||||
| chr4:55636741-55636890 | Rare:26 | ||||
| chr4:55637120-55637470 | Common:5; Rare:51 | ||||
| chr4:55853469-55853739 | Rare:72 | ||||
| chr4:55948721-55948961 | Common:1; Rare:49 | ||||
| chr4:55949071-55949355 | Common:1; Rare:71 |