| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:164956891-164957006 | Rare:35 | ||||
| chr4:165112818-165113015 | Common:1; Rare:57 | ||||
| chr4:165327388-165327741 | Common:3; Rare:105 | ||||
| chr4:168318740-168318871 | Rare:28 | ||||
| chr4:168480452-168480797 | Common:1; Rare:56 | ||||
| chr4:168894394-168894675 | Rare:58; Clinvar:1; Clinvar (benign):3 | ||||
| chr4:168921381-168921734 | Common:1; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:169010239-169010496 | Common:1; Rare:78 | ||||
| chr4:169620360-169620760 | Common:2; Rare:136 | ||||
| chr4:169757869-169758069 | Rare:58 | ||||
| chr4:170026305-170026599 | Common:4; Rare:113 | ||||
| chr4:170027310-170027509 | Common:3; Rare:50 | ||||
| chr4:173334261-173334740 | Rare:121 | ||||
| chr4:173369784-173369882 | Rare:30 | ||||
| chr4:173370690-173370975 | Common:2; Rare:73 |