| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38181798-38182048 | Common:2; Rare:63 | ||||
| chr22:38506275-38506619 | Common:1; Rare:112 | ||||
| chr22:38656372-38656713 | Common:1; Rare:87 | ||||
| chr22:38681810-38682030 | Common:2; Rare:95 | ||||
| chr22:38794072-38794315 | Common:1; Rare:64 | ||||
| chr22:38872189-38872464 | Rare:73 | ||||
| chr22:38982170-38982438 | Common:2; Rare:58 | ||||
| chr22:39244954-39245277 | Common:1; Rare:70 | ||||
| chr22:39319594-39319768 | Common:3; Rare:81 | ||||
| chr22:39399518-39399805 | Common:4; Rare:104 | ||||
| chr22:39502140-39502412 | Rare:80 | ||||
| chr22:40044174-40044346 | Common:2; Rare:36 | ||||
| chr22:40346434-40346664 | Rare:106; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:40636633-40637033 | Common:2; Rare:113 | ||||
| chr22:40856434-40857159 | Common:2; Rare:295; Clinvar:3 |