| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:44676936-44676982 | Common:1; Rare:9 | ||||
| chr22:44677016-44677177 | Common:3; Rare:28 | ||||
| chr22:45163735-45163948 | Common:3; Rare:78 | ||||
| chr22:45212355-45212595 | Common:3; Rare:61 | ||||
| chr22:45309672-45309990 | Common:1; Rare:126 | ||||
| chr22:45413519-45413746 | Common:1; Rare:89 | ||||
| chr22:45502548-45502923 | Common:2; Rare:107 | ||||
| chr22:46053773-46053869 | Rare:38 | ||||
| chr22:46250245-46250408 | Common:2; Rare:49 | ||||
| chr22:46296744-46296939 | Rare:62 | ||||
| chr22:46335509-46335769 | Common:3; Rare:97; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:46537623-46537827 | Common:2; Rare:77 | ||||
| chr22:46738170-46738425 | Common:5; Rare:63 | ||||
| chr22:46762496-46762712 | Common:3; Rare:82 | ||||
| chr22:48489548-48489597 | Rare:17 |