| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44939882-44940061 | Common:2; Rare:52 | ||||
| chr21:45287875-45288087 | Common:6; Rare:84 | ||||
| chr21:45404887-45405178 | Common:12; Rare:172 | ||||
| chr21:45981490-45981808 | Common:23; Rare:72; Clinvar (benign):2 | ||||
| chr21:46002377-46002685 | Common:2; Rare:99; Clinvar:10; Clinvar (benign):6 | ||||
| chr21:46286256-46286406 | Common:4; Rare:56 | ||||
| chr22:17628591-17628920 | Common:2; Rare:113 | ||||
| chr22:19432284-19432610 | Common:4; Rare:140 | ||||
| chr22:19447694-19447855 | Common:2; Rare:59 | ||||
| chr22:19941720-19942134 | Common:2; Rare:115; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20116952-20117557 | Common:4; Rare:174 | ||||
| chr22:20495787-20495994 | Common:2; Rare:77 | ||||
| chr22:20982201-20982353 | Common:2; Rare:34; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002126-21002220 | Common:1; Rare:31 | ||||
| chr22:21642055-21642331 | Common:2; Rare:81 |