| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208266121-208266248 | Common:3; Rare:42 | ||||
| chr2:210002433-210002659 | Common:6; Rare:77 | ||||
| chr2:210171233-210171543 | Common:4; Rare:119 | ||||
| chr2:210476675-210476820 | Rare:54 | ||||
| chr2:213284238-213284483 | Rare:79 | ||||
| chr2:214809234-214809404 | Common:1; Rare:52; Clinvar (benign):2 | ||||
| chr2:214809620-214809992 | Common:3; Rare:134; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:215311888-215312133 | Common:8; Rare:97 | ||||
| chr2:216081766-216081904 | Common:1; Rare:45 | ||||
| chr2:216498732-216498898 | Common:6; Rare:74 | ||||
| chr2:218217052-218217226 | Common:1; Rare:63 | ||||
| chr2:218270104-218270538 | Common:5; Rare:133; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218292496-218292685 | Common:1; Rare:56 | ||||
| chr2:218399601-218399678 | Common:1; Rare:32 | ||||
| chr2:218568296-218568659 | Common:3; Rare:98 |