| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:144645858-144646213 | Common:1; Rare:100 | ||||
| chr4:144646565-144646945 | Rare:115 | ||||
| chr4:144647202-144647226 | Rare:4 | ||||
| chr4:145098141-145098361 | Rare:77 | ||||
| chr4:145480477-145480777 | Common:1; Rare:54 | ||||
| chr4:145481490-145481690 | Rare:47 | ||||
| chr4:145481693-145481743 | Rare:11 | ||||
| chr4:145482494-145482815 | Common:2; Rare:88 | ||||
| chr4:145482836-145483092 | Rare:50 | ||||
| chr4:145545879-145546061 | Rare:34 | ||||
| chr4:145619296-145619396 | Rare:47 | ||||
| chr4:147617254-147617479 | Common:1; Rare:48 | ||||
| chr4:147684127-147684289 | Rare:66 | ||||
| chr4:148442375-148442712 | Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:152679889-152680120 | Rare:75 |