| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147731932-147732357 | Common:1; Rare:153 | ||||
| chr4:148442319-148442749 | Rare:126; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:151015216-151015398 | Rare:49 | ||||
| chr4:151015718-151015844 | Rare:61 | ||||
| chr4:151099477-151099713 | Common:3; Rare:93 | ||||
| chr4:151100313-151100587 | Common:1; Rare:54 | ||||
| chr4:151226347-151226554 | Rare:38 | ||||
| chr4:151408880-151409267 | Common:5; Rare:122 | ||||
| chr4:152352688-152352932 | Rare:63 | ||||
| chr4:152536052-152536407 | Common:2; Rare:136 | ||||
| chr4:152779711-152780160 | Common:2; Rare:115 | ||||
| chr4:153204370-153204464 | Rare:21 | ||||
| chr4:154491780-154492042 | Common:1; Rare:53 | ||||
| chr4:154550372-154550530 | Rare:47 | ||||
| chr4:156970907-156971229 | Common:1; Rare:55 |