| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145179594-145179734 | Rare:46 | ||||
| chr4:145180455-145180813 | Common:1; Rare:101 | ||||
| chr4:145481667-145481703 | Rare:9 | ||||
| chr4:145619340-145619436 | Rare:37; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:145938782-145938961 | Rare:48 | ||||
| chr4:146522333-146522460 | Common:2; Rare:51 | ||||
| chr4:146945722-146946024 | Rare:82 | ||||
| chr4:147617198-147617661 | Common:1; Rare:97 | ||||
| chr4:147684081-147684316 | Common:1; Rare:97 | ||||
| chr4:147731434-147731683 | Common:3; Rare:60 | ||||
| chr4:147732217-147732441 | Rare:80 | ||||
| chr4:148368398-148368685 | Common:1; Rare:57 | ||||
| chr4:148442350-148442751 | Rare:119; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:151015205-151015297 | Rare:30 | ||||
| chr4:151015485-151015812 | Rare:101 |