| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36328718-36328921 | Rare:49 | ||||
| chr22:36481595-36481729 | Common:2; Rare:35 | ||||
| chr22:36529105-36529515 | Common:6; Rare:126 | ||||
| chr22:37560315-37560540 | Common:1; Rare:72 | ||||
| chr22:37849301-37849459 | Rare:95 | ||||
| chr22:37953591-37953797 | Rare:81 | ||||
| chr22:38057688-38057834 | Common:1; Rare:30 | ||||
| chr22:38201739-38202111 | Common:2; Rare:106 | ||||
| chr22:38505656-38505730 | Rare:24 | ||||
| chr22:38570184-38570438 | Common:4; Rare:41 | ||||
| chr22:38656360-38656677 | Common:1; Rare:81 | ||||
| chr22:38681845-38681997 | Rare:65 | ||||
| chr22:38738958-38739013 | Rare:18; Clinvar (benign):2 | ||||
| chr22:38742467-38742748 | Common:1; Rare:92 | ||||
| chr22:38872171-38872471 | Rare:80 |