| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68252492-68252861 | Common:3; Rare:114 | ||||
| chr2:68467239-68467746 | Common:2; Rare:139 | ||||
| chr2:69387173-69387384 | Rare:54; Clinvar:2 | ||||
| chr2:69437428-69437527 | Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:69437566-69437644 | Common:1; Rare:46; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:69643616-69643834 | Rare:79 | ||||
| chr2:69742012-69742157 | Rare:31 | ||||
| chr2:69829524-69829737 | Common:1; Rare:85 | ||||
| chr2:69914906-69915198 | Common:1; Rare:69 | ||||
| chr2:69961442-69961951 | Common:1; Rare:161; Clinvar:1 | ||||
| chr2:70086931-70087056 | Common:1; Rare:72 | ||||
| chr2:70087337-70087878 | Common:2; Rare:191 | ||||
| chr2:70087882-70088555 | Common:1; Rare:177 | ||||
| chr2:70248455-70248809 | Common:5; Rare:139 | ||||
| chr2:70257978-70258242 | Common:2; Rare:93 |