| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45287875-45288093 | Common:6; Rare:85 | ||||
| chr21:45404874-45405200 | Common:13; Rare:183 | ||||
| chr21:45981519-45981824 | Common:23; Rare:70; Clinvar (benign):2 | ||||
| chr21:45987017-45987175 | Common:1; Rare:60; Clinvar:9; Clinvar (benign):4 | ||||
| chr21:46002286-46002583 | Common:2; Rare:94; Clinvar:12; Clinvar (benign):7 | ||||
| chr21:46184413-46184725 | Common:3; Rare:28 | ||||
| chr21:46286256-46286392 | Common:4; Rare:51 | ||||
| chr21:46323789-46324199 | Common:2; Rare:149; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46458649-46459063 | Common:3; Rare:144 | ||||
| chr22:17159185-17159395 | Common:5; Rare:104 | ||||
| chr22:17628694-17628872 | Common:1; Rare:62 | ||||
| chr22:17638684-17638840 | Rare:54 | ||||
| chr22:17774400-17774550 | Rare:54 | ||||
| chr22:18024488-18024693 | Common:1; Rare:57 | ||||
| chr22:18077802-18078022 | Common:5; Rare:70; Clinvar:3; Clinvar (benign):2 |