| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45287879-45288073 | Common:5; Rare:74 | ||||
| chr21:46635457-46635696 | Common:6; Rare:82 | ||||
| chr22:20117260-20117583 | Common:2; Rare:101 | ||||
| chr22:21002106-21002201 | Common:3; Rare:29 | ||||
| chr22:24555884-24556066 | Rare:53 | ||||
| chr22:26512425-26512550 | Common:1; Rare:56 | ||||
| chr22:28741800-28742058 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:29267955-29268328 | Common:2; Rare:107 | ||||
| chr22:29553633-29553938 | Common:3; Rare:101 | ||||
| chr22:30356876-30356985 | Common:1; Rare:35 | ||||
| chr22:37849320-37849443 | Rare:69 | ||||
| chr22:37953581-37953742 | Rare:66 | ||||
| chr22:38656382-38656678 | Common:1; Rare:70 | ||||
| chr22:38681817-38682008 | Common:1; Rare:81 | ||||
| chr22:40346445-40346550 | Rare:43; Clinvar:2; Clinvar (benign):1 |