| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:41981654-41981789 | Common:2; Rare:42 | ||||
| chr4:41990396-41990573 | Common:1; Rare:64 | ||||
| chr4:42656943-42657225 | Common:7; Rare:100 | ||||
| chr4:44678369-44678706 | Common:1; Rare:125 | ||||
| chr4:44726523-44726637 | Rare:45 | ||||
| chr4:47463647-47463817 | Common:2; Rare:56 | ||||
| chr4:47485198-47485340 | Common:1; Rare:53 | ||||
| chr4:47838099-47838208 | Common:1; Rare:17 | ||||
| chr4:47913857-47913946 | Rare:28 | ||||
| chr4:48016509-48016780 | Common:3; Rare:72 | ||||
| chr4:48269787-48269981 | Common:2; Rare:44 | ||||
| chr4:48341202-48341578 | Common:2; Rare:155 | ||||
| chr4:48780236-48780558 | Common:2; Rare:97 | ||||
| chr4:48986128-48986358 | Rare:62 | ||||
| chr4:52038246-52038405 | Rare:56; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 |