| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188292987-188293090 | Rare:18 | ||||
| chr2:188974173-188974582 | Rare:101; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189003408-189003787 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr2:189007823-189008142 | Rare:98; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):16 | ||||
| chr2:189441133-189441504 | Common:2; Rare:109 | ||||
| chr2:189783973-189784123 | Common:3; Rare:57; Clinvar (benign):1 | ||||
| chr2:189784268-189784512 | Common:3; Rare:83; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:190880588-190880897 | Common:4; Rare:108 | ||||
| chr2:191014133-191014374 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245219-191245570 | Common:3; Rare:115 | ||||
| chr2:191677831-191678218 | Common:4; Rare:110 | ||||
| chr2:196068804-196068925 | Common:1; Rare:33 | ||||
| chr2:197434970-197435320 | Rare:107 | ||||
| chr2:197453100-197453571 | Rare:158 | ||||
| chr2:197453848-197454021 | Rare:48 |