Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70088010-70088503 | Common:1; Rare:134 | ||||
chr2:71454445-71454734 | Rare:55 | ||||
chr2:73893799-73893982 | Common:3; Rare:36 | ||||
chr2:73894258-73894335 | Rare:11 | ||||
chr2:73899545-73899793 | Common:1; Rare:40 | ||||
chr2:73916547-73916914 | Common:4; Rare:74 | ||||
chr2:74120203-74120385 | Rare:66 | ||||
chr2:74377431-74377689 | Common:1; Rare:64 | ||||
chr2:85537925-85537967 | Rare:11 | ||||
chr2:85543487-85543780 | Rare:51; Clinvar (benign):1 | ||||
chr2:86251957-86252217 | Common:1; Rare:59; Clinvar:4; Clinvar (benign):4 | ||||
chr2:88016540-88016817 | Common:10; Rare:118 | ||||
chr2:91659921-91660045 | Rare:22 | ||||
chr2:94586990-94587298 | Rare:78 | ||||
chr2:95526702-95526832 | Common:1; Rare:47 |