Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58558525-58558737 | Rare:63 | ||||
chr19:58573294-58573695 | Common:3; Rare:101 | ||||
chr2:264561-264967 | Common:4; Rare:148 | ||||
chr2:3377780-3377937 | Rare:44 | ||||
chr2:3379611-3379780 | Common:2; Rare:71 | ||||
chr2:3519520-3519663 | Common:1; Rare:35 | ||||
chr2:3558262-3558489 | Common:5; Rare:96 | ||||
chr2:3575128-3575354 | Common:2; Rare:65; Clinvar:3; Clinvar (benign):5 | ||||
chr2:6866524-6866734 | Rare:34 | ||||
chr2:6917331-6917475 | Rare:54 | ||||
chr2:8682632-8682907 | Common:8; Rare:108 | ||||
chr2:8837563-8837717 | Common:1; Rare:60 | ||||
chr2:9423219-9423697 | Rare:136 | ||||
chr2:9474498-9474623 | Common:6; Rare:58 | ||||
chr2:9555615-9556002 | Common:2; Rare:131 |