| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44711175-44711315 | Rare:44 | ||||
| chr21:44711550-44711960 | Common:1; Rare:114 | ||||
| chr21:44801705-44802005 | Common:1; Rare:246 | ||||
| chr21:44817937-44818287 | Common:3; Rare:349 | ||||
| chr21:44818204-44818604 | Common:4; Rare:216 | ||||
| chr21:44872257-44872695 | Common:6; Rare:185 | ||||
| chr21:44873598-44874088 | Common:21; Rare:484 | ||||
| chr21:44939816-44940154 | Common:12; Rare:221 | ||||
| chr21:44940155-44940555 | Common:2; Rare:111 | ||||
| chr21:45073383-45073949 | Common:14; Rare:275 | ||||
| chr21:45074304-45074796 | Common:11; Rare:549 | ||||
| chr21:45287753-45288144 | Common:18; Rare:397 | ||||
| chr21:45404931-45405257 | Common:36; Rare:495 | ||||
| chr21:45405492-45405731 | Rare:184 | ||||
| chr21:45455362-45455666 | Common:2; Rare:135; Clinvar:1; Clinvar (benign):2 |