| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169612546-169612783 | Common:5; Rare:80; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:169620368-169620707 | Common:4; Rare:213 | ||||
| chr4:169757873-169758078 | Rare:59 | ||||
| chr4:170026274-170026624 | Common:8; Rare:261 | ||||
| chr4:170027115-170027751 | Common:10; Rare:284 | ||||
| chr4:173334327-173334782 | Rare:172 | ||||
| chr4:173335031-173335441 | Common:6; Rare:185 | ||||
| chr4:173370661-173370999 | Common:4; Rare:163 | ||||
| chr4:174283611-174284023 | Common:2; Rare:165 | ||||
| chr4:174522476-174522780 | Common:2; Rare:132; Clinvar:8 | ||||
| chr4:176319720-176320070 | Common:9; Rare:233 | ||||
| chr4:176320380-176320730 | Common:2; Rare:165 | ||||
| chr4:177309702-177309938 | Common:2; Rare:74 | ||||
| chr4:177442376-177442554 | Rare:191; Clinvar:4 | ||||
| chr4:182917211-182917561 | Common:8; Rare:220 |