| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44801707-44801893 | Rare:71 | ||||
| chr21:44865953-44866061 | Common:1; Rare:21 | ||||
| chr21:44873506-44874063 | Common:9; Rare:212 | ||||
| chr21:45287828-45288093 | Common:6; Rare:106 | ||||
| chr21:45404861-45405194 | Common:12; Rare:183 | ||||
| chr21:45455236-45455530 | Common:2; Rare:98 | ||||
| chr21:45493294-45493558 | Common:2; Rare:76; Clinvar:1 | ||||
| chr21:45505127-45505372 | Common:4; Rare:138; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr21:45505727-45505916 | Common:1; Rare:89 | ||||
| chr21:45981501-45981946 | Common:24; Rare:119; Clinvar:5; Clinvar (benign):4 | ||||
| chr21:45986523-45987004 | Common:6; Rare:162; Clinvar:22; Clinvar (benign):11 | ||||
| chr21:45987006-45987175 | Common:1; Rare:61; Clinvar:9; Clinvar (benign):4 | ||||
| chr21:45987197-45987519 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):4 | ||||
| chr21:46002024-46002401 | Common:2; Rare:128; Clinvar:16; Clinvar (benign):14 | ||||
| chr21:46098020-46098166 | Rare:52; Clinvar (benign):1 |