| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:143513160-143513790 | Common:14; Rare:865 | ||||
| chr4:143904655-143905536 | Common:15; Rare:271 | ||||
| chr4:144019226-144019701 | Common:10; Rare:169 | ||||
| chr4:144140595-144141009 | Common:12; Rare:168 | ||||
| chr4:145097680-145097990 | Rare:137 | ||||
| chr4:145098044-145098444 | Rare:615 | ||||
| chr4:145177521-145178622 | Common:7; Rare:473 | ||||
| chr4:145179240-145179990 | Rare:665 | ||||
| chr4:145180391-145181195 | Common:6; Rare:730 | ||||
| chr4:145618429-145619082 | Common:6; Rare:253 | ||||
| chr4:145619151-145619706 | Common:13; Rare:947; Clinvar:18; Clinvar (benign):6 | ||||
| chr4:145732870-145733340 | Common:8; Rare:346 | ||||
| chr4:146175466-146175866 | Common:3; Rare:182 | ||||
| chr4:146176136-146176336 | Common:3; Rare:48 | ||||
| chr4:146520829-146521358 | Common:3; Rare:142 |