| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37849311-37849476 | Rare:94 | ||||
| chr22:38181804-38182048 | Common:2; Rare:63 | ||||
| chr22:38505978-38506050 | Rare:27 | ||||
| chr22:38506281-38506619 | Common:1; Rare:107 | ||||
| chr22:38656391-38656714 | Common:1; Rare:72 | ||||
| chr22:38681827-38682090 | Common:2; Rare:106 | ||||
| chr22:38754427-38754678 | Common:2; Rare:50 | ||||
| chr22:38872180-38872421 | Rare:64 | ||||
| chr22:39319594-39319745 | Common:3; Rare:74 | ||||
| chr22:39502141-39502417 | Rare:83 | ||||
| chr22:40346445-40346692 | Common:1; Rare:106; Clinvar:12; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:40819260-40819484 | Common:11; Rare:114 | ||||
| chr22:40856431-40857167 | Common:3; Rare:299; Clinvar:4 | ||||
| chr22:41285980-41286049 | Common:1; Rare:19 | ||||
| chr22:41286117-41286557 | Common:2; Rare:143 |