| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:49334507-49334543 | Rare:6 | ||||
| chr22:50314233-50314410 | Common:2; Rare:79 | ||||
| chr22:50465034-50465241 | Common:1; Rare:85; Clinvar (pathogenic):1 | ||||
| chr22:50466205-50466418 | Rare:81 | ||||
| chr22:50756755-50756966 | Common:7; Rare:106 | ||||
| chr22:50757094-50757248 | Common:1; Rare:49 | ||||
| chr3:9396212-9396322 | Rare:43 | ||||
| chr3:9396636-9396878 | Common:1; Rare:95 | ||||
| chr3:9396992-9397085 | Common:1; Rare:28 | ||||
| chr3:9398473-9398626 | Rare:36 | ||||
| chr3:9399935-9400016 | Rare:21 | ||||
| chr3:10017766-10017937 | Common:2; Rare:44 | ||||
| chr3:10962122-10962248 | Rare:13 | ||||
| chr3:10977874-10978141 | Rare:54 | ||||
| chr3:10994429-10994467 | Common:1; Rare:6 |