| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37608679-37608890 | Common:1; Rare:62 | ||||
| chr22:37675400-37675710 | Common:4; Rare:89 | ||||
| chr22:37849300-37849476 | Rare:104 | ||||
| chr22:37953609-37953806 | Rare:76 | ||||
| chr22:38057359-38057520 | Common:1; Rare:43 | ||||
| chr22:38181775-38182040 | Common:2; Rare:64 | ||||
| chr22:38201687-38202138 | Common:2; Rare:123 | ||||
| chr22:38656372-38656706 | Common:1; Rare:85 | ||||
| chr22:38681847-38682017 | Common:1; Rare:75 | ||||
| chr22:38755418-38755551 | Common:1; Rare:27 | ||||
| chr22:38872191-38872440 | Rare:69 | ||||
| chr22:39349746-39350007 | Common:1; Rare:77 | ||||
| chr22:39502138-39502386 | Rare:68 | ||||
| chr22:40276589-40276743 | Rare:38 | ||||
| chr22:40346445-40346630 | Rare:87; Clinvar:9; Clinvar (benign):5; Clinvar (pathogenic):1 |