| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:144645882-144646158 | Common:1; Rare:75 | ||||
| chr4:145098124-145098361 | Rare:78 | ||||
| chr4:145180449-145180882 | Common:1; Rare:122 | ||||
| chr4:145480654-145480777 | Common:1; Rare:23 | ||||
| chr4:145481407-145481716 | Common:2; Rare:68 | ||||
| chr4:145482942-145483042 | Rare:19 | ||||
| chr4:145545887-145546153 | Common:1; Rare:46 | ||||
| chr4:145619320-145619403 | Rare:33; Clinvar (benign):1 | ||||
| chr4:145938782-145938965 | Rare:49 | ||||
| chr4:146522327-146522474 | Common:4; Rare:57 | ||||
| chr4:147617190-147617503 | Common:1; Rare:73 | ||||
| chr4:147684073-147684302 | Common:1; Rare:88 | ||||
| chr4:148442323-148442715 | Rare:112; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:148444693-148445121 | Common:3; Rare:101 | ||||
| chr4:150581722-150581988 | Rare:55 |