| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:165327411-165327741 | Common:2; Rare:95 | ||||
| chr4:165327864-165327911 | Common:1; Rare:12 | ||||
| chr4:168480464-168480574 | Rare:19 | ||||
| chr4:168831852-168832106 | Common:2; Rare:63 | ||||
| chr4:169010053-169010483 | Common:6; Rare:135 | ||||
| chr4:169612562-169612753 | Common:4; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:169620360-169620760 | Common:2; Rare:136 | ||||
| chr4:169660023-169660282 | Common:1; Rare:51 | ||||
| chr4:169660302-169660479 | Common:1; Rare:32 | ||||
| chr4:169660484-169660583 | Rare:22 | ||||
| chr4:169757837-169758075 | Common:2; Rare:75 | ||||
| chr4:170026297-170026623 | Common:4; Rare:129 | ||||
| chr4:170027173-170027605 | Common:4; Rare:106 | ||||
| chr4:170089281-170089485 | Common:1; Rare:52 | ||||
| chr4:173168183-173168272 | Rare:22 |