Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:181891665-181892096 | Common:4; Rare:174 | ||||
chr2:183124252-183124449 | Common:4; Rare:65 | ||||
chr2:186486037-186486344 | Common:3; Rare:86 | ||||
chr2:186590072-186590350 | Rare:82 | ||||
chr2:188974268-188974568 | Rare:75; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr2:188991665-188991869 | Rare:56; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):10 | ||||
chr2:189003382-189003786 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
chr2:189441181-189441517 | Common:2; Rare:101 | ||||
chr2:189783956-189784078 | Common:2; Rare:39 | ||||
chr2:189784305-189784506 | Common:3; Rare:65; Clinvar:6; Clinvar (benign):1 | ||||
chr2:190880619-190880857 | Common:4; Rare:80 | ||||
chr2:191014124-191014333 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191677856-191678147 | Common:4; Rare:82 | ||||
chr2:197434973-197435181 | Rare:71 | ||||
chr2:197453247-197453561 | Rare:108 |