| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68365137-68365390 | Common:2; Rare:47 | ||||
| chr2:68387467-68387579 | Common:1; Rare:14 | ||||
| chr2:68467262-68467605 | Common:1; Rare:88 | ||||
| chr2:68735076-68735412 | Common:3; Rare:71 | ||||
| chr2:69437428-69437725 | Common:1; Rare:132; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:69741900-69742164 | Common:1; Rare:61 | ||||
| chr2:69829460-69829735 | Common:1; Rare:111 | ||||
| chr2:69902543-69902865 | Common:4; Rare:82 | ||||
| chr2:70087368-70088019 | Common:2; Rare:218 | ||||
| chr2:70293657-70293902 | Common:3; Rare:80 | ||||
| chr2:71068534-71068679 | Rare:66 | ||||
| chr2:71130225-71130736 | Common:7; Rare:152; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071707-73071841 | Common:2; Rare:49 | ||||
| chr2:73214146-73214275 | Common:1; Rare:42 | ||||
| chr2:73284218-73284554 | Common:1; Rare:89 |