| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151015704-151015861 | Rare:74 | ||||
| chr4:151099497-151099623 | Common:1; Rare:47 | ||||
| chr4:152679959-152680102 | Rare:21 | ||||
| chr4:152779552-152780193 | Common:4; Rare:154 | ||||
| chr4:158671825-158672383 | Common:5; Rare:142; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:158723207-158723471 | Common:2; Rare:113 | ||||
| chr4:163494611-163494754 | Common:1; Rare:44 | ||||
| chr4:169010205-169010464 | Common:1; Rare:80 | ||||
| chr4:169660036-169660294 | Common:1; Rare:46 | ||||
| chr4:169757860-169758084 | Rare:64 | ||||
| chr4:173370683-173370962 | Common:2; Rare:70 | ||||
| chr4:174283631-174284025 | Common:1; Rare:85 | ||||
| chr4:176319721-176320074 | Common:5; Rare:119 | ||||
| chr4:176729256-176729565 | Common:2; Rare:65 | ||||
| chr4:177442336-177442518 | Common:1; Rare:108; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |