| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216694457-216694478 | Rare:3 | ||||
| chr2:216694504-216694833 | Rare:84 | ||||
| chr2:216695523-216695580 | Rare:11 | ||||
| chr2:217813672-217813960 | Common:1; Rare:73 | ||||
| chr2:217885727-217885862 | Common:1; Rare:39 | ||||
| chr2:217894978-217895083 | Rare:32 | ||||
| chr2:217919982-217920150 | Common:3; Rare:39 | ||||
| chr2:217937361-217937764 | Rare:85 | ||||
| chr2:217978769-217978914 | Common:1; Rare:44 | ||||
| chr2:218217115-218217246 | Rare:54 | ||||
| chr2:218249567-218249837 | Rare:72 | ||||
| chr2:218270054-218270538 | Common:5; Rare:151; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218282109-218282404 | Common:3; Rare:60 | ||||
| chr2:218381906-218382374 | Common:2; Rare:92 | ||||
| chr2:218568293-218568669 | Common:4; Rare:98 |