Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:177552943-177553142 | Common:3; Rare:61 | ||||
chr2:178450696-178450886 | Common:1; Rare:65 | ||||
chr2:178451067-178451382 | Common:6; Rare:90; Clinvar:4; Clinvar (benign):3 | ||||
chr2:178478531-178478676 | Common:1; Rare:45 | ||||
chr2:179264514-179264626 | Rare:43 | ||||
chr2:179861312-179861491 | Rare:68 | ||||
chr2:180980246-180980637 | Common:1; Rare:127 | ||||
chr2:180980719-180980971 | Rare:67 | ||||
chr2:181457219-181457390 | Rare:64 | ||||
chr2:181891943-181892230 | Common:2; Rare:102 | ||||
chr2:182715887-182716480 | Common:3; Rare:193 | ||||
chr2:182716862-182717069 | Common:1; Rare:38 | ||||
chr2:182866556-182866707 | Common:1; Rare:37 | ||||
chr2:182867121-182867211 | Rare:24 | ||||
chr2:183038014-183038432 | Common:2; Rare:117 |