Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:226652445-226652715 | Rare:54 | ||||
chr2:226726026-226726203 | Common:3; Rare:38 | ||||
chr2:226787365-226787560 | Common:1; Rare:28 | ||||
chr2:226790739-226790854 | Rare:24 | ||||
chr2:226796562-226797036 | Common:1; Rare:156; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr2:226797200-226797503 | Common:2; Rare:102; Clinvar (benign):1 | ||||
chr2:226797643-226797960 | Rare:106 | ||||
chr2:226800571-226800713 | Rare:31 | ||||
chr2:226801785-226802105 | Common:1; Rare:68 | ||||
chr2:226811119-226811280 | Common:1; Rare:30 | ||||
chr2:226811678-226811703 | Rare:2 | ||||
chr2:226888074-226888281 | Common:1; Rare:31 | ||||
chr2:227341205-227341291 | Rare:21 | ||||
chr2:227342790-227343088 | Common:2; Rare:74; Clinvar (benign):1 | ||||
chr2:227345944-227346043 | Common:1; Rare:15 |