| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207437780-207438047 | Rare:51 | ||||
| chr2:210599486-210599820 | Rare:66; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:215397690-215397986 | Common:1; Rare:73 | ||||
| chr2:215439105-215439341 | Common:3; Rare:40 | ||||
| chr2:215773291-215773411 | Rare:19 | ||||
| chr2:215998673-215998982 | Common:3; Rare:48 | ||||
| chr2:216012096-216012296 | Common:4; Rare:34 | ||||
| chr2:216017522-216017742 | Common:1; Rare:39 | ||||
| chr2:217160969-217161157 | Common:7; Rare:25 | ||||
| chr2:217162554-217163015 | Common:2; Rare:94 | ||||
| chr2:218402616-218402714 | Rare:37 | ||||
| chr2:219685024-219685291 | Common:2; Rare:77 | ||||
| chr2:221103897-221104245 | Common:2; Rare:60 | ||||
| chr2:221124896-221125167 | Common:3; Rare:63 | ||||
| chr2:221196557-221196666 | Common:2; Rare:16 |