| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:16898565-16898888 | Common:14; Rare:59 | ||||
| chr4:17512055-17512195 | Common:3; Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:17614564-17614651 | Common:2; Rare:39 | ||||
| chr4:17810619-17811086 | Common:4; Rare:143 | ||||
| chr4:20252762-20252890 | Common:1; Rare:30 | ||||
| chr4:20700259-20700502 | Common:1; Rare:106 | ||||
| chr4:20983918-20984193 | Common:2; Rare:54 | ||||
| chr4:21303908-21304122 | Common:17; Rare:68 | ||||
| chr4:23890042-23890173 | Rare:19 | ||||
| chr4:25160367-25160710 | Common:3; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234007 | Rare:64 | ||||
| chr4:25312646-25312809 | Common:1; Rare:47 | ||||
| chr4:25914029-25914321 | Common:2; Rare:126 | ||||
| chr4:26319774-26319888 | Rare:33 | ||||
| chr4:26320590-26320877 | Common:1; Rare:117 |