| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45404941-45405170 | Common:12; Rare:144 | ||||
| chr21:45493051-45493206 | Common:1; Rare:57 | ||||
| chr21:45981500-45981944 | Common:24; Rare:118; Clinvar:5; Clinvar (benign):4 | ||||
| chr21:46097845-46098166 | Common:3; Rare:100; Clinvar (benign):1 | ||||
| chr21:46184423-46184756 | Common:4; Rare:29 | ||||
| chr21:46286209-46286662 | Common:6; Rare:152 | ||||
| chr21:46323784-46324225 | Common:3; Rare:170; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458686-46459084 | Common:4; Rare:136 | ||||
| chr21:46635457-46635737 | Common:6; Rare:95 | ||||
| chr22:17159207-17159393 | Common:4; Rare:96 | ||||
| chr22:17628648-17628860 | Common:2; Rare:73 | ||||
| chr22:17638684-17638837 | Rare:53 | ||||
| chr22:17774390-17774585 | Rare:68 | ||||
| chr22:18077780-18078014 | Common:4; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19178445-19178527 | Common:1; Rare:22 |