| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:41214454-41214742 | Common:5; Rare:70 | ||||
| chr4:41256728-41257120 | Common:4; Rare:128; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41261759-41261929 | Rare:66 | ||||
| chr4:41935000-41935309 | Common:3; Rare:82 | ||||
| chr4:41990389-41990585 | Common:1; Rare:70 | ||||
| chr4:44678276-44678731 | Common:3; Rare:168 | ||||
| chr4:44726547-44726671 | Rare:54 | ||||
| chr4:47463647-47463817 | Common:2; Rare:56 | ||||
| chr4:47485166-47485371 | Common:1; Rare:68 | ||||
| chr4:47914505-47914684 | Common:1; Rare:60 | ||||
| chr4:48016638-48016784 | Common:1; Rare:43 | ||||
| chr4:48269795-48270021 | Common:2; Rare:50 | ||||
| chr4:48341225-48341478 | Common:1; Rare:105 | ||||
| chr4:48780223-48780572 | Common:3; Rare:103 | ||||
| chr4:48830821-48831229 | Common:1; Rare:129 |