| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44873634-44874043 | Common:8; Rare:161 | ||||
| chr21:45287879-45288060 | Common:5; Rare:68 | ||||
| chr21:46323814-46324131 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr22:17628706-17628872 | Common:1; Rare:56 | ||||
| chr22:17638677-17638760 | Rare:25 | ||||
| chr22:19447690-19447876 | Common:2; Rare:71 | ||||
| chr22:19479687-19479960 | Common:4; Rare:76 | ||||
| chr22:20117252-20117561 | Common:3; Rare:94 | ||||
| chr22:21002106-21002205 | Common:3; Rare:31 | ||||
| chr22:24555829-24556037 | Rare:67 | ||||
| chr22:26512439-26512550 | Common:1; Rare:51 | ||||
| chr22:28741806-28742078 | Common:2; Rare:79 | ||||
| chr22:29267950-29268339 | Common:2; Rare:115 | ||||
| chr22:29581089-29581211 | Common:2; Rare:34 | ||||
| chr22:29767056-29767392 | Common:4; Rare:103 |