| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68467269-68467649 | Common:1; Rare:104 | ||||
| chr2:68529527-68529655 | Rare:23 | ||||
| chr2:68774713-68774947 | Common:1; Rare:41 | ||||
| chr2:69013055-69013412 | Common:9; Rare:83 | ||||
| chr2:69387183-69387423 | Rare:70; Clinvar:2 | ||||
| chr2:69437385-69437522 | Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:69437598-69437697 | Rare:44; Clinvar:2 | ||||
| chr2:69643611-69643883 | Rare:100 | ||||
| chr2:69741724-69741973 | Common:3; Rare:37 | ||||
| chr2:69829551-69829948 | Common:2; Rare:128 | ||||
| chr2:69893900-69894016 | Rare:34 | ||||
| chr2:69915337-69915574 | Rare:47 | ||||
| chr2:70086914-70087066 | Common:1; Rare:83 | ||||
| chr2:70190871-70191127 | Common:1; Rare:61 | ||||
| chr2:70248495-70248816 | Common:5; Rare:126 |