| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:40629467-40629953 | Common:1; Rare:106 | ||||
| chr4:41256733-41256970 | Common:3; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:41934982-41935248 | Common:3; Rare:78 | ||||
| chr4:41990389-41990580 | Common:1; Rare:69 | ||||
| chr4:44678356-44678731 | Common:1; Rare:140 | ||||
| chr4:44726487-44726648 | Common:2; Rare:57 | ||||
| chr4:46123953-46124187 | Common:3; Rare:43 | ||||
| chr4:47485198-47485407 | Common:2; Rare:67 | ||||
| chr4:47914569-47914967 | Common:3; Rare:115 | ||||
| chr4:48016634-48016796 | Common:1; Rare:48 | ||||
| chr4:48269790-48269981 | Common:2; Rare:42 | ||||
| chr4:48341280-48341494 | Rare:89 | ||||
| chr4:48780245-48780572 | Common:2; Rare:97 | ||||
| chr4:48831656-48831664 | Rare:3 | ||||
| chr4:51842813-51843212 | Common:1; Rare:118 |