| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43955300-43955589 | Common:3; Rare:85 | ||||
| chr22:44024146-44024360 | Common:1; Rare:70 | ||||
| chr22:44181095-44181374 | Common:5; Rare:60 | ||||
| chr22:44498179-44498479 | Common:2; Rare:116 | ||||
| chr22:44668458-44668751 | Common:4; Rare:109 | ||||
| chr22:45163661-45164015 | Common:4; Rare:126 | ||||
| chr22:45413621-45413742 | Rare:41 | ||||
| chr22:46053778-46053901 | Rare:43 | ||||
| chr22:46250245-46250408 | Common:2; Rare:49 | ||||
| chr22:46267841-46268072 | Common:1; Rare:79 | ||||
| chr22:46296750-46296918 | Rare:54 | ||||
| chr22:46335601-46335797 | Common:5; Rare:91; Clinvar:9; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46377591-46377807 | Common:3; Rare:53 | ||||
| chr22:46762455-46762676 | Common:3; Rare:83 | ||||
| chr22:49918378-49918680 | Common:2; Rare:110; Clinvar (benign):1 |