Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:152717829-152717957 | Rare:53 | ||||
chr2:152718538-152718627 | Rare:35 | ||||
chr2:159712417-159712534 | Common:2; Rare:50 | ||||
chr2:161308348-161308519 | Common:2; Rare:45 | ||||
chr2:171434014-171434225 | Common:1; Rare:56 | ||||
chr2:174248481-174248758 | Common:1; Rare:88 | ||||
chr2:175181664-175181762 | Common:3; Rare:41 | ||||
chr2:177392680-177392808 | Rare:34; Clinvar:1 | ||||
chr2:183124150-183124411 | Common:5; Rare:68 | ||||
chr2:186486099-186486344 | Common:3; Rare:79 | ||||
chr2:189784319-189784512 | Common:2; Rare:61; Clinvar:6 | ||||
chr2:191677878-191678140 | Common:4; Rare:67 | ||||
chr2:197499817-197500144 | Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197500234-197500416 | Common:1; Rare:75 | ||||
chr2:201071688-201072008 | Rare:60 |