| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38057357-38057520 | Common:1; Rare:45 | ||||
| chr22:38181744-38181958 | Common:2; Rare:57; Clinvar:1 | ||||
| chr22:38505996-38506104 | Common:1; Rare:43 | ||||
| chr22:38506159-38506592 | Common:1; Rare:152 | ||||
| chr22:38570184-38570493 | Common:5; Rare:56 | ||||
| chr22:38656348-38656687 | Common:1; Rare:89 | ||||
| chr22:38681799-38681987 | Common:1; Rare:77 | ||||
| chr22:38739407-38739472 | Common:1; Rare:14 | ||||
| chr22:38739776-38740169 | Rare:94; Clinvar (benign):1 | ||||
| chr22:38872186-38872414 | Rare:63 | ||||
| chr22:39040575-39040926 | Common:1; Rare:68 | ||||
| chr22:39241128-39241193 | Rare:15 | ||||
| chr22:39244976-39245236 | Rare:57 | ||||
| chr22:39319594-39319768 | Common:3; Rare:81 | ||||
| chr22:39349784-39350008 | Common:1; Rare:69 |