| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39697932-39698203 | Common:2; Rare:118 | ||||
| chr4:40056662-40056941 | Common:4; Rare:92 | ||||
| chr4:40629762-40629917 | Common:1; Rare:45 | ||||
| chr4:40630130-40630232 | Common:1; Rare:14 | ||||
| chr4:41935000-41935187 | Common:3; Rare:48 | ||||
| chr4:41990390-41990566 | Common:1; Rare:65 | ||||
| chr4:44678382-44678679 | Common:1; Rare:109 | ||||
| chr4:44726547-44726642 | Rare:38 | ||||
| chr4:48016624-48016784 | Common:1; Rare:47 | ||||
| chr4:48269802-48269985 | Common:1; Rare:38 | ||||
| chr4:48906712-48906871 | Rare:37 | ||||
| chr4:51842822-51843212 | Common:1; Rare:116 | ||||
| chr4:52659268-52659394 | Common:1; Rare:44 | ||||
| chr4:53365959-53366164 | Rare:44 | ||||
| chr4:55346169-55346347 | Common:3; Rare:62; Clinvar:3; Clinvar (benign):2 |