| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189580366-189580874 | Common:3; Rare:149; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:189580880-189580957 | Rare:27 | ||||
| chr2:189783956-189784133 | Common:3; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189784260-189784537 | Common:4; Rare:99; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190180651-190181046 | Rare:115 | ||||
| chr2:190290403-190290576 | Common:1; Rare:45; Clinvar (pathogenic):1 | ||||
| chr2:190343791-190344060 | Rare:62 | ||||
| chr2:190344083-190344159 | Common:2; Rare:18 | ||||
| chr2:190469212-190469853 | Common:12; Rare:114 | ||||
| chr2:190489617-190489866 | Common:2; Rare:52 | ||||
| chr2:190534656-190534853 | Common:1; Rare:65 | ||||
| chr2:190648709-190648913 | Common:1; Rare:74 | ||||
| chr2:190880644-190880900 | Common:4; Rare:89 | ||||
| chr2:190881100-190881448 | Common:2; Rare:139 | ||||
| chr2:191014070-191014353 | Common:2; Rare:95; Clinvar:2; Clinvar (benign):3 |