| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:41767046-41767182 | Common:3; Rare:63; Clinvar:1 | ||||
| chr21:41879295-41879541 | Common:5; Rare:80 | ||||
| chr21:42496173-42496744 | Common:2; Rare:140; Clinvar:1 | ||||
| chr21:42499548-42499679 | Common:3; Rare:28 | ||||
| chr21:42879532-42879669 | Common:3; Rare:43 | ||||
| chr21:42893033-42893351 | Common:4; Rare:113 | ||||
| chr21:42974214-42974652 | Common:1; Rare:160 | ||||
| chr21:43659433-43659636 | Common:1; Rare:66 | ||||
| chr21:43728591-43728905 | Common:3; Rare:81 | ||||
| chr21:43740679-43741072 | Common:7; Rare:129 | ||||
| chr21:43776204-43776611 | Common:5; Rare:143; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43789414-43789630 | Common:1; Rare:86 | ||||
| chr21:43946874-43946999 | Common:1; Rare:23 | ||||
| chr21:43950540-43950667 | Common:1; Rare:35 | ||||
| chr21:44107129-44107396 | Common:5; Rare:45 |