| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35399915-35400217 | Rare:102 | ||||
| chr22:35961563-35961761 | Common:1; Rare:35 | ||||
| chr22:36285665-36285956 | Rare:108; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:36387818-36387909 | Rare:16 | ||||
| chr22:36388065-36388374 | Common:2; Rare:83 | ||||
| chr22:36512615-36512679 | Rare:17 | ||||
| chr22:37019423-37019858 | Common:5; Rare:124 | ||||
| chr22:37231356-37231461 | Rare:32 | ||||
| chr22:37608392-37608496 | Common:2; Rare:36 | ||||
| chr22:37675348-37675712 | Common:4; Rare:105 | ||||
| chr22:37843829-37843873 | Rare:11 | ||||
| chr22:37844279-37844605 | Common:2; Rare:94 | ||||
| chr22:37849293-37849482 | Rare:114 | ||||
| chr22:37906054-37906357 | Common:1; Rare:80 | ||||
| chr22:37953569-37953803 | Rare:90 |