| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139301295-139301616 | Common:4; Rare:98 | ||||
| chr4:139453665-139453760 | Common:2; Rare:35 | ||||
| chr4:139453762-139454190 | Common:3; Rare:110; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556181-139556362 | Rare:42 | ||||
| chr4:140373393-140373701 | Common:2; Rare:127 | ||||
| chr4:140523932-140524231 | Common:2; Rare:92 | ||||
| chr4:141220825-141220934 | Rare:34 | ||||
| chr4:142846279-142846437 | Rare:40 | ||||
| chr4:143337105-143337195 | Rare:39 | ||||
| chr4:143513451-143513723 | Common:1; Rare:84 | ||||
| chr4:145098130-145098350 | Rare:73 | ||||
| chr4:145481614-145481703 | Rare:26 | ||||
| chr4:145482869-145483001 | Rare:21 | ||||
| chr4:145619340-145619396 | Rare:19 | ||||
| chr4:147617243-147617446 | Common:1; Rare:45 |