| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:209577929-209578108 | Rare:25 | ||||
| chr2:209578345-209578745 | Common:10; Rare:114 | ||||
| chr2:209663046-209663446 | Rare:88 | ||||
| chr2:209872700-209873020 | Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:211404168-211404318 | Rare:51 | ||||
| chr2:211744470-211744790 | Common:1; Rare:65 | ||||
| chr2:211762732-211763132 | Common:4; Rare:105 | ||||
| chr2:211982429-211982829 | Common:3; Rare:104 | ||||
| chr2:212154418-212154818 | Common:3; Rare:82 | ||||
| chr2:212427614-212428014 | Rare:110 | ||||
| chr2:212536503-212536625 | Rare:24 | ||||
| chr2:212537087-212537293 | Common:5; Rare:53 | ||||
| chr2:212537432-212537832 | Common:4; Rare:137 | ||||
| chr2:212913357-212913757 | Common:8; Rare:89 | ||||
| chr2:213188209-213188609 | Common:3; Rare:97 |