Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:175181629-175181765 | Common:4; Rare:59 | ||||
chr2:176002221-176002420 | Common:3; Rare:86 | ||||
chr2:176188524-176188668 | Common:1; Rare:51 | ||||
chr2:177212613-177212802 | Common:1; Rare:82 | ||||
chr2:177263415-177263703 | Common:1; Rare:68 | ||||
chr2:177263821-177264151 | Common:2; Rare:88 | ||||
chr2:177264533-177264854 | Common:2; Rare:92 | ||||
chr2:177392672-177393070 | Common:2; Rare:139; Clinvar:6; Clinvar (benign):4 | ||||
chr2:177552750-177552838 | Common:1; Rare:32 | ||||
chr2:177618699-177619013 | Common:7; Rare:85 | ||||
chr2:178451090-178451369 | Common:6; Rare:83; Clinvar:4; Clinvar (benign):3 | ||||
chr2:178478507-178478659 | Common:1; Rare:47 | ||||
chr2:180980246-180980545 | Common:1; Rare:94 | ||||
chr2:181457239-181457536 | Common:2; Rare:111 | ||||
chr2:183078658-183078797 | Rare:29 |