| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145482869-145483001 | Rare:21 | ||||
| chr4:145545889-145546061 | Rare:33 | ||||
| chr4:145619328-145619403 | Rare:28; Clinvar (benign):1 | ||||
| chr4:147480921-147481144 | Common:1; Rare:48 | ||||
| chr4:147617235-147617482 | Common:1; Rare:53 | ||||
| chr4:147684096-147684289 | Common:1; Rare:76 | ||||
| chr4:148442333-148442712 | Rare:109; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:150581765-150581973 | Rare:44 | ||||
| chr4:151015216-151015289 | Rare:25 | ||||
| chr4:151226361-151226560 | Rare:36 | ||||
| chr4:151408856-151409193 | Common:5; Rare:108 | ||||
| chr4:151760972-151761156 | Rare:64 | ||||
| chr4:152536054-152536276 | Rare:85 | ||||
| chr4:152679935-152680144 | Rare:49 | ||||
| chr4:152779796-152780120 | Common:2; Rare:85 |