| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203224287-203224606 | Rare:60 | ||||
| chr2:203225057-203225159 | Common:1; Rare:13 | ||||
| chr2:203773095-203773129 | Rare:8 | ||||
| chr2:204897407-204897631 | Rare:33 | ||||
| chr2:206059097-206059309 | Rare:39 | ||||
| chr2:206084477-206084616 | Common:1; Rare:26 | ||||
| chr2:206766509-206766779 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:207081882-207082118 | Common:2; Rare:54 | ||||
| chr2:207117410-207117430 | Rare:4 | ||||
| chr2:207117438-207117512 | Rare:11 | ||||
| chr2:207120176-207120314 | Rare:21 | ||||
| chr2:207120753-207120807 | Rare:15 | ||||
| chr2:207120833-207121048 | Rare:31 | ||||
| chr2:207151894-207152066 | Common:1; Rare:28 | ||||
| chr2:207163360-207163809 | Common:2; Rare:78 |