| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:138242203-138242617 | Common:2; Rare:82 | ||||
| chr4:139301295-139301557 | Common:4; Rare:81 | ||||
| chr4:139453674-139453696 | Rare:9 | ||||
| chr4:139453972-139454190 | Common:3; Rare:62; Clinvar:5; Clinvar (benign):4 | ||||
| chr4:139556391-139556651 | Rare:40 | ||||
| chr4:139665966-139666022 | Common:1; Rare:20 | ||||
| chr4:140373358-140373709 | Common:3; Rare:140 | ||||
| chr4:141220794-141220954 | Rare:51 | ||||
| chr4:142405404-142405599 | Common:1; Rare:32 | ||||
| chr4:142474385-142474571 | Rare:29 | ||||
| chr4:143184672-143184985 | Common:8; Rare:121 | ||||
| chr4:145098130-145098361 | Rare:77 | ||||
| chr4:145619355-145619396 | Rare:14 | ||||
| chr4:146521859-146521976 | Rare:25 | ||||
| chr4:147617254-147617473 | Common:1; Rare:48 |