| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169611810-169612258 | Rare:144; Clinvar:2 | ||||
| chr4:169612192-169612332 | Rare:29 | ||||
| chr4:169612238-169613050 | Common:36; Rare:627; Clinvar:27; Clinvar (benign):11 | ||||
| chr4:169620087-169620828 | Common:14; Rare:943 | ||||
| chr4:169620885-169621388 | Rare:170 | ||||
| chr4:169659208-169659667 | Common:5; Rare:136 | ||||
| chr4:169659934-169660485 | Common:8; Rare:386 | ||||
| chr4:169660509-169660914 | Rare:111 | ||||
| chr4:169662105-169662510 | Common:2; Rare:85 | ||||
| chr4:169757743-169758234 | Common:7; Rare:507 | ||||
| chr4:170006639-170007490 | Common:8; Rare:307 | ||||
| chr4:170026261-170026636 | Common:22; Rare:636 | ||||
| chr4:170026555-170027570 | Common:18; Rare:604 | ||||
| chr4:171812469-171812964 | Common:6; Rare:193 | ||||
| chr4:171813161-171813561 | Common:3; Rare:149 |