| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:23889904-23889977 | Rare:13 | ||||
| chr4:23889988-23890133 | Rare:25 | ||||
| chr4:23903964-23904368 | Rare:72 | ||||
| chr4:24584248-24584346 | Rare:35 | ||||
| chr4:24584459-24584725 | Common:1; Rare:82 | ||||
| chr4:25160356-25160725 | Common:3; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233837-25234050 | Rare:91 | ||||
| chr4:25312508-25312860 | Common:2; Rare:120 | ||||
| chr4:25376979-25377350 | Common:3; Rare:113 | ||||
| chr4:26319426-26319794 | Rare:104 | ||||
| chr4:26320584-26320838 | Common:1; Rare:97 | ||||
| chr4:26320900-26321041 | Rare:49; Clinvar (benign):1 | ||||
| chr4:26583971-26584131 | Rare:34 | ||||
| chr4:26857504-26857758 | Common:4; Rare:76 | ||||
| chr4:26860563-26860819 | Common:2; Rare:85 |