| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:187448242-187448407 | Rare:25 | ||||
| chr2:188291672-188291998 | Common:3; Rare:89 | ||||
| chr2:188292692-188292863 | Common:1; Rare:42 | ||||
| chr2:188974260-188974564 | Rare:76; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189007940-189008142 | Rare:69; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):12 | ||||
| chr2:189441078-189441511 | Common:2; Rare:133 | ||||
| chr2:189580759-189580925 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783965-189784078 | Common:2; Rare:38 | ||||
| chr2:189784276-189784537 | Common:4; Rare:93; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190534645-190534955 | Common:3; Rare:98 | ||||
| chr2:190648725-190648912 | Rare:69 | ||||
| chr2:191014123-191014333 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245231-191245606 | Common:4; Rare:119 | ||||
| chr2:191677853-191678173 | Common:4; Rare:93 | ||||
| chr2:191678565-191678614 | Rare:24 |