Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:177552761-177552807 | Rare:23 | ||||
chr2:178450727-178451024 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):2 | ||||
chr2:178451083-178451381 | Common:6; Rare:86; Clinvar:4; Clinvar (benign):3 | ||||
chr2:178478515-178478659 | Common:1; Rare:45 | ||||
chr2:181891626-181892021 | Common:4; Rare:165 | ||||
chr2:182715930-182716481 | Common:3; Rare:179 | ||||
chr2:183124252-183124449 | Common:4; Rare:65 | ||||
chr2:186485988-186486391 | Common:3; Rare:117 | ||||
chr2:186589894-186590034 | Rare:40 | ||||
chr2:186590224-186590355 | Rare:39 | ||||
chr2:188291549-188292143 | Common:8; Rare:161 | ||||
chr2:188292644-188292972 | Common:1; Rare:77 | ||||
chr2:188293005-188293078 | Rare:10 | ||||
chr2:189441050-189441517 | Common:3; Rare:152 | ||||
chr2:189580762-189580938 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):2 |