| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:145735254-145735681 | Common:8; Rare:126; Clinvar:16; Clinvar (benign):12 | ||||
| chr6:145814685-145814922 | Common:1; Rare:111 | ||||
| chr6:145964276-145964549 | Common:1; Rare:92 | ||||
| chr6:148342438-148342623 | Rare:40 | ||||
| chr6:149546001-149546148 | Rare:62 | ||||
| chr6:149718058-149718151 | Common:1; Rare:30 | ||||
| chr6:149746476-149746643 | Common:2; Rare:82 | ||||
| chr6:149749658-149749847 | Rare:94 | ||||
| chr6:149750301-149750416 | Common:1; Rare:21 | ||||
| chr6:150866330-150866595 | Rare:99 | ||||
| chr6:151391491-151391799 | Common:3; Rare:84 | ||||
| chr6:151452005-151452555 | Common:5; Rare:191; Clinvar (benign):3 | ||||
| chr6:151690505-151690568 | Rare:12 | ||||
| chr6:152302102-152302221 | Rare:34 | ||||
| chr6:152982964-152983331 | Common:2; Rare:115 |