| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38181810-38182064 | Common:2; Rare:67 | ||||
| chr22:38506281-38506592 | Common:1; Rare:101 | ||||
| chr22:38570181-38570465 | Common:4; Rare:51 | ||||
| chr22:38656391-38656682 | Common:1; Rare:64 | ||||
| chr22:38681821-38682030 | Common:2; Rare:88 | ||||
| chr22:38794088-38794338 | Common:1; Rare:64 | ||||
| chr22:39319596-39319921 | Common:4; Rare:122 | ||||
| chr22:39349791-39350019 | Common:1; Rare:72 | ||||
| chr22:39399624-39399796 | Common:3; Rare:66 | ||||
| chr22:39502141-39502386 | Rare:67 | ||||
| chr22:39532668-39532917 | Common:2; Rare:109 | ||||
| chr22:40044136-40044341 | Common:2; Rare:46 | ||||
| chr22:40044579-40044869 | Common:2; Rare:65 | ||||
| chr22:40346434-40346556 | Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40370457-40370664 | Rare:83 |