Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:178478527-178478663 | Common:1; Rare:43 | ||||
chr2:181457195-181457558 | Common:2; Rare:131 | ||||
chr2:181457982-181458278 | Common:1; Rare:85 | ||||
chr2:182715887-182716017 | Rare:28 | ||||
chr2:182716206-182716328 | Rare:47 | ||||
chr2:183124298-183124485 | Rare:69 | ||||
chr2:186486024-186486354 | Common:3; Rare:94 | ||||
chr2:189783960-189784125 | Common:3; Rare:62; Clinvar (benign):1 | ||||
chr2:189784305-189784512 | Common:3; Rare:68; Clinvar:6; Clinvar (benign):1 | ||||
chr2:191014143-191014353 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191677847-191678173 | Common:4; Rare:94 | ||||
chr2:195656856-195657249 | Common:2; Rare:110 | ||||
chr2:196176277-196176459 | Rare:23 | ||||
chr2:196639553-196639757 | Rare:67 | ||||
chr2:197434999-197435174 | Rare:59 |