| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45404983-45405222 | Common:10; Rare:148 | ||||
| chr21:45405539-45405674 | Rare:44 | ||||
| chr21:45981516-45981937 | Common:24; Rare:110; Clinvar:5; Clinvar (benign):4 | ||||
| chr21:45987506-45987651 | Rare:66; Clinvar:8; Clinvar (benign):4 | ||||
| chr21:46113293-46113579 | Common:1; Rare:62 | ||||
| chr21:46286230-46286408 | Common:4; Rare:67 | ||||
| chr21:46286582-46286644 | Common:1; Rare:20 | ||||
| chr21:46323830-46324166 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46458685-46459055 | Common:3; Rare:126 | ||||
| chr22:17159223-17159357 | Common:4; Rare:61 | ||||
| chr22:17628615-17628872 | Common:2; Rare:86 | ||||
| chr22:19291696-19291887 | Common:9; Rare:59 | ||||
| chr22:19431698-19431813 | Rare:27 | ||||
| chr22:19432288-19432591 | Common:4; Rare:128 | ||||
| chr22:19447686-19447942 | Common:2; Rare:102 |