| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:186590097-186590349 | Rare:73 | ||||
| chr2:187554344-187554531 | Rare:38 | ||||
| chr2:189441137-189441529 | Common:2; Rare:126 | ||||
| chr2:189783965-189784112 | Common:3; Rare:54; Clinvar (benign):1 | ||||
| chr2:189784276-189784557 | Common:4; Rare:98; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343868-190343960 | Rare:18 | ||||
| chr2:190880644-190880834 | Common:3; Rare:61 | ||||
| chr2:191014109-191014357 | Common:2; Rare:91; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677854-191678197 | Common:4; Rare:97 | ||||
| chr2:196799603-196799787 | Common:1; Rare:56 | ||||
| chr2:197434973-197435176 | Rare:70 | ||||
| chr2:197453239-197453554 | Rare:106 | ||||
| chr2:197499792-197500424 | Common:2; Rare:240; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:200811308-200811614 | Common:1; Rare:98 | ||||
| chr2:200864623-200864788 | Rare:64 |