| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:38121346-38121542 | Common:1; Rare:71 | ||||
| chr21:38498436-38498517 | Rare:10 | ||||
| chr21:39445751-39445874 | Common:3; Rare:37 | ||||
| chr21:42893110-42893336 | Common:1; Rare:74 | ||||
| chr21:44873771-44874032 | Common:7; Rare:97 | ||||
| chr21:45287867-45288085 | Common:6; Rare:87 | ||||
| chr21:45981529-45981818 | Common:23; Rare:65; Clinvar (benign):2 | ||||
| chr21:46286266-46286399 | Common:3; Rare:47 | ||||
| chr21:46323813-46324161 | Common:2; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46635497-46635723 | Common:5; Rare:77 | ||||
| chr22:17159175-17159385 | Common:6; Rare:99 | ||||
| chr22:17628689-17628884 | Common:1; Rare:71 | ||||
| chr22:17774415-17774574 | Rare:57 | ||||
| chr22:18077820-18078007 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19122395-19122681 | Common:3; Rare:65 |