| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151099427-151099709 | Common:3; Rare:108 | ||||
| chr4:152679870-152680165 | Rare:98 | ||||
| chr4:152779721-152780013 | Common:1; Rare:82 | ||||
| chr4:153204293-153204463 | Rare:34 | ||||
| chr4:154550372-154550505 | Rare:41 | ||||
| chr4:156971014-156971279 | Common:1; Rare:42 | ||||
| chr4:156971779-156972090 | Common:2; Rare:107 | ||||
| chr4:158671849-158672313 | Common:5; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723335-158723439 | Common:2; Rare:49 | ||||
| chr4:163494464-163494745 | Common:2; Rare:109 | ||||
| chr4:165327400-165327915 | Common:3; Rare:144 | ||||
| chr4:168480458-168480510 | Rare:12 | ||||
| chr4:169010239-169010474 | Common:1; Rare:71 | ||||
| chr4:169620385-169620697 | Common:2; Rare:109 | ||||
| chr4:169660069-169660282 | Common:1; Rare:40 |