| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36344688-36344916 | Common:1; Rare:39 | ||||
| chr22:36355034-36355329 | Common:1; Rare:56 | ||||
| chr22:36370591-36370773 | Rare:40 | ||||
| chr22:36376641-36376825 | Common:4; Rare:35 | ||||
| chr22:36385586-36385610 | Rare:3 | ||||
| chr22:36386044-36386316 | Common:1; Rare:43 | ||||
| chr22:36386524-36386624 | Common:2; Rare:18 | ||||
| chr22:36387383-36387509 | Common:1; Rare:36 | ||||
| chr22:36649632-36649709 | Rare:9 | ||||
| chr22:36879922-36880149 | Common:2; Rare:44 | ||||
| chr22:36929402-36929682 | Rare:80 | ||||
| chr22:36930499-36930812 | Common:2; Rare:99; Clinvar (benign):1 | ||||
| chr22:37255083-37255315 | Common:1; Rare:34 | ||||
| chr22:37482792-37483073 | Rare:52 | ||||
| chr22:37546085-37546238 | Common:1; Rare:27 |