| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36157244-36157397 | Rare:34 | ||||
| chr22:36387934-36388336 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:37019423-37019848 | Common:5; Rare:122 | ||||
| chr22:37244152-37244367 | Rare:58 | ||||
| chr22:37849292-37849475 | Rare:110 | ||||
| chr22:37953597-37953741 | Rare:63 | ||||
| chr22:38180903-38181080 | Rare:39 | ||||
| chr22:38201753-38202110 | Common:2; Rare:102 | ||||
| chr22:38570169-38570501 | Common:5; Rare:62 | ||||
| chr22:38656366-38656723 | Common:1; Rare:92 | ||||
| chr22:38681813-38682030 | Common:2; Rare:93 | ||||
| chr22:38755779-38756003 | Common:1; Rare:54 | ||||
| chr22:39014024-39014315 | Common:2; Rare:71 | ||||
| chr22:39020787-39021170 | Common:2; Rare:93 | ||||
| chr22:39319590-39319838 | Common:3; Rare:100 |