| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139177159-139177456 | Rare:86 | ||||
| chr4:139280085-139280273 | Common:1; Rare:62 | ||||
| chr4:139301231-139301593 | Common:4; Rare:104 | ||||
| chr4:139302448-139302752 | Common:2; Rare:70 | ||||
| chr4:139453743-139454350 | Common:3; Rare:182; Clinvar:12; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr4:139556103-139556292 | Rare:46 | ||||
| chr4:139665697-139666076 | Common:2; Rare:92 | ||||
| chr4:140373314-140373736 | Common:3; Rare:161 | ||||
| chr4:140756313-140756435 | Rare:24 | ||||
| chr4:141132786-141132917 | Rare:46 | ||||
| chr4:141636785-141636930 | Common:1; Rare:32 | ||||
| chr4:143184851-143184958 | Common:5; Rare:40 | ||||
| chr4:143513637-143514098 | Common:2; Rare:181 | ||||
| chr4:144645916-144646288 | Common:3; Rare:95 | ||||
| chr4:145098130-145098404 | Rare:87 |