| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42363245-42363857 | Common:8; Rare:320 | ||||
| chr21:42364186-42365345 | Common:14; Rare:641 | ||||
| chr21:42367510-42367714 | Rare:53 | ||||
| chr21:42370899-42371410 | Common:9; Rare:184 | ||||
| chr21:42374368-42375831 | Common:26; Rare:626; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr21:42376106-42376648 | Common:3; Rare:359; Clinvar:15; Clinvar (benign):12 | ||||
| chr21:42376690-42377130 | Common:8; Rare:153 | ||||
| chr21:42381365-42381886 | Common:9; Rare:176 | ||||
| chr21:42389631-42389738 | Common:1; Rare:19 | ||||
| chr21:42449889-42450289 | Common:11; Rare:126 | ||||
| chr21:42516109-42516912 | Common:6; Rare:197 | ||||
| chr21:42524706-42525007 | Common:2; Rare:67 | ||||
| chr21:42614871-42615320 | Common:5; Rare:146 | ||||
| chr21:42781360-42781810 | Common:11; Rare:98 | ||||
| chr21:42784210-42784830 | Common:9; Rare:105 |