| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:143513292-143513936 | Common:4; Rare:228 | ||||
| chr4:143513938-143514101 | Common:1; Rare:70 | ||||
| chr4:144645926-144646175 | Common:1; Rare:68 | ||||
| chr4:144646295-144646723 | Common:2; Rare:97 | ||||
| chr4:145098115-145098359 | Rare:80 | ||||
| chr4:145481657-145481716 | Rare:12 | ||||
| chr4:145619320-145619406 | Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:147617242-147617597 | Common:1; Rare:74 | ||||
| chr4:147684081-147684302 | Common:1; Rare:87 | ||||
| chr4:147732025-147732345 | Rare:119 | ||||
| chr4:148442272-148442736 | Rare:136; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:150581810-150581944 | Rare:27 | ||||
| chr4:151015204-151015417 | Rare:57 | ||||
| chr4:151015709-151015775 | Rare:28 | ||||
| chr4:151099427-151099713 | Common:3; Rare:108 |