| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46285591-46285896 | Common:3; Rare:70 | ||||
| chr21:46286163-46286734 | Common:7; Rare:188 | ||||
| chr21:46286847-46286917 | Rare:19 | ||||
| chr21:46323786-46324202 | Common:2; Rare:152; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46324353-46324920 | Common:9; Rare:209 | ||||
| chr21:46325160-46325422 | Common:2; Rare:90 | ||||
| chr21:46458437-46459139 | Common:6; Rare:214 | ||||
| chr21:46635019-46635197 | Common:2; Rare:41 | ||||
| chr21:46635402-46635716 | Common:8; Rare:121 | ||||
| chr21:46635904-46636092 | Common:2; Rare:54 | ||||
| chr22:17084673-17085110 | Common:5; Rare:146; Clinvar:5; Clinvar (benign):3 | ||||
| chr22:17085216-17085433 | Common:2; Rare:73; Clinvar:2 | ||||
| chr22:17158538-17158627 | Rare:23 | ||||
| chr22:17158665-17158735 | Common:1; Rare:13 | ||||
| chr22:17158882-17159033 | Common:3; Rare:45 |