Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:178451090-178451353 | Common:6; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
chr2:178478507-178478659 | Common:1; Rare:47 | ||||
chr2:179264514-179264857 | Common:4; Rare:128 | ||||
chr2:180980270-180980545 | Common:1; Rare:86 | ||||
chr2:181457237-181457565 | Common:2; Rare:119 | ||||
chr2:182715935-182716369 | Common:3; Rare:148 | ||||
chr2:183124252-183124452 | Common:4; Rare:67 | ||||
chr2:186486130-186486344 | Common:3; Rare:71 | ||||
chr2:188291812-188291939 | Common:1; Rare:46 | ||||
chr2:189179707-189179789 | Rare:8; Clinvar:1 | ||||
chr2:189441094-189441438 | Common:1; Rare:86 | ||||
chr2:189783965-189784123 | Common:3; Rare:60; Clinvar (benign):1 | ||||
chr2:189784276-189784537 | Common:4; Rare:93; Clinvar:8; Clinvar (benign):2 | ||||
chr2:190319761-190319983 | Common:4; Rare:75; Clinvar (benign):3 | ||||
chr2:190534688-190534853 | Common:1; Rare:56 |