| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:21146941-21147164 | Common:4; Rare:53 | ||||
| chr21:25342151-25342296 | Rare:23 | ||||
| chr21:29231843-29232055 | Rare:42 | ||||
| chr21:37221292-37221422 | Common:2; Rare:59 | ||||
| chr21:44517319-44517617 | Common:2; Rare:99 | ||||
| chr21:45319623-45319825 | Common:2; Rare:43 | ||||
| chr21:45992188-45992372 | Common:1; Rare:62; Clinvar:6; Clinvar (benign):2 | ||||
| chr22:19881968-19882158 | Common:2; Rare:30 | ||||
| chr22:22298046-22298209 | Common:2; Rare:68 | ||||
| chr22:30246002-30246197 | Common:1; Rare:32 | ||||
| chr22:36288884-36289228 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:46069870-46070056 | Rare:42 | ||||
| chr3:40453163-40453417 | Common:6; Rare:56 | ||||
| chr3:57959958-57960178 | Common:3; Rare:35 | ||||
| chr3:75435020-75435372 | Common:4; Rare:123 |