Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:177618699-177618784 | Common:1; Rare:35 | ||||
chr2:178451098-178451357 | Common:5; Rare:77; Clinvar:3; Clinvar (benign):3 | ||||
chr2:178478515-178478659 | Common:1; Rare:45 | ||||
chr2:186486130-186486376 | Common:3; Rare:85 | ||||
chr2:186590254-186590349 | Rare:30 | ||||
chr2:187554312-187554514 | Rare:42 | ||||
chr2:188293007-188293023 | Rare:4 | ||||
chr2:189441133-189441511 | Common:2; Rare:116 | ||||
chr2:189783965-189784125 | Common:3; Rare:61; Clinvar (benign):1 | ||||
chr2:189784281-189784540 | Common:4; Rare:94; Clinvar:8; Clinvar (benign):2 | ||||
chr2:190319756-190319929 | Common:3; Rare:55; Clinvar (benign):4 | ||||
chr2:190343868-190344043 | Rare:34 | ||||
chr2:190534688-190534896 | Common:1; Rare:66 | ||||
chr2:190648709-190648881 | Common:1; Rare:69 | ||||
chr2:190880637-190880863 | Common:4; Rare:80 |