Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87342283-87342410 | Common:3; Rare:39 | ||||
chr10:95414894-95415114 | Rare:38 | ||||
chr10:99431383-99431678 | Common:1; Rare:55 | ||||
chr10:102109111-102109445 | Rare:86 | ||||
chr10:103892318-103892642 | Common:1; Rare:58 | ||||
chr10:107032482-107032759 | Common:3; Rare:62 | ||||
chr10:114515734-114515786 | Rare:12 | ||||
chr11:1841029-1841523 | Common:1; Rare:152; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr11:1926477-1926703 | Common:3; Rare:73; Clinvar:1 | ||||
chr11:1934577-1934919 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):2 | ||||
chr11:1995874-1996000 | Common:1; Rare:29 | ||||
chr11:1996053-1996214 | Common:2; Rare:50 | ||||
chr11:2138251-2138397 | Common:1; Rare:34 | ||||
chr11:2147752-2148025 | Common:2; Rare:58 | ||||
chr11:2148696-2148855 | Common:1; Rare:32 |