| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143450666-143450929 | Common:1; Rare:98; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511632-143511834 | Common:4; Rare:47 | ||||
| chr6:144095548-144095753 | Common:4; Rare:59 | ||||
| chr6:144285153-144285396 | Common:3; Rare:69 | ||||
| chr6:145814680-145814921 | Common:1; Rare:112 | ||||
| chr6:145964286-145964443 | Common:1; Rare:52 | ||||
| chr6:149545979-149546167 | Common:1; Rare:82 | ||||
| chr6:149718066-149718188 | Common:2; Rare:46 | ||||
| chr6:149746502-149746642 | Common:2; Rare:67 | ||||
| chr6:149749664-149749796 | Rare:77 | ||||
| chr6:151452030-151452548 | Common:4; Rare:183 | ||||
| chr6:152983009-152983315 | Common:2; Rare:97 | ||||
| chr6:152983518-152983744 | Common:3; Rare:87 | ||||
| chr6:153002652-153002838 | Common:3; Rare:67 | ||||
| chr6:153131219-153131474 | Rare:112 |