| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50293532-50293585 | Rare:13 | ||||
| chr22:50314506-50314628 | Common:1; Rare:55 | ||||
| chr22:50437310-50437560 | Common:2; Rare:76 | ||||
| chr22:50462410-50462707 | Common:5; Rare:126; Clinvar (benign):1 | ||||
| chr22:50517769-50518051 | Common:1; Rare:91 | ||||
| chr22:50527672-50527749 | Rare:27; Clinvar (benign):3 | ||||
| chr22:50541244-50541389 | Common:5; Rare:22 | ||||
| chr22:50672429-50672780 | Common:9; Rare:84 | ||||
| chr22:50714466-50714547 | Rare:20 | ||||
| chr22:50723936-50724237 | Common:1; Rare:73 | ||||
| chr22:50725646-50725924 | Common:3; Rare:46 | ||||
| chr22:50726399-50726755 | Common:1; Rare:76 | ||||
| chr22:50728080-50728216 | Common:1; Rare:17 | ||||
| chr22:50728836-50728985 | Rare:22 | ||||
| chr3:4817926-4818240 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):3 |