| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:20983907-20984038 | Common:1; Rare:24 | ||||
| chr4:20984118-20984220 | Common:1; Rare:29 | ||||
| chr4:22516040-22516250 | Common:2; Rare:67 | ||||
| chr4:23890030-23890233 | Common:1; Rare:31 | ||||
| chr4:24584463-24584721 | Common:1; Rare:78 | ||||
| chr4:25160336-25160727 | Common:3; Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233834-25234063 | Rare:95 | ||||
| chr4:25312605-25312861 | Common:2; Rare:93 | ||||
| chr4:25376964-25377350 | Common:4; Rare:115 | ||||
| chr4:25914029-25914392 | Common:3; Rare:157 | ||||
| chr4:26320564-26320832 | Common:1; Rare:98 | ||||
| chr4:26320905-26321043 | Rare:49; Clinvar (benign):1 | ||||
| chr4:26583971-26584153 | Rare:38 | ||||
| chr4:26857494-26857776 | Common:4; Rare:85 | ||||
| chr4:30720237-30720437 | Common:1; Rare:51 |