| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216081737-216081952 | Common:1; Rare:71 | ||||
| chr2:216412705-216412785 | Rare:11 | ||||
| chr2:216498704-216498904 | Common:7; Rare:89 | ||||
| chr2:216694423-216694858 | Rare:105 | ||||
| chr2:216695219-216695656 | Common:1; Rare:81 | ||||
| chr2:217434108-217434448 | Rare:75 | ||||
| chr2:217905391-217905691 | Rare:60 | ||||
| chr2:217978622-217978763 | Rare:40 | ||||
| chr2:217978766-217978981 | Common:1; Rare:64 | ||||
| chr2:218002825-218003096 | Common:2; Rare:72 | ||||
| chr2:218217058-218217248 | Common:1; Rare:68 | ||||
| chr2:218269398-218269669 | Rare:98 | ||||
| chr2:218270054-218270602 | Common:5; Rare:176; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:218285670-218285823 | Common:1; Rare:25 | ||||
| chr2:218287265-218287361 | Rare:16 |