| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37806227-37806612 | Common:4; Rare:69 | ||||
| chr22:37888234-37888429 | Common:1; Rare:34 | ||||
| chr22:38314581-38314709 | Rare:32 | ||||
| chr22:38374907-38374996 | Rare:10 | ||||
| chr22:38738371-38738671 | Rare:58 | ||||
| chr22:38741534-38741845 | Common:2; Rare:63 | ||||
| chr22:39243933-39244166 | Rare:78 | ||||
| chr22:40401477-40401672 | Common:1; Rare:46 | ||||
| chr22:40402077-40402201 | Rare:30 | ||||
| chr22:40403161-40403245 | Rare:15 | ||||
| chr22:40635251-40635414 | Common:1; Rare:34 | ||||
| chr22:40829619-40829707 | Rare:20 | ||||
| chr22:41092461-41092637 | Rare:85 | ||||
| chr22:41092852-41092899 | Rare:13; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:41129967-41130226 | Rare:47 |