Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:67482906-67483154 | Rare:55; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr11:68030378-68030744 | Common:3; Rare:103; Clinvar:1; Clinvar (benign):2 | ||||
chr11:68038915-68039060 | Rare:43; Clinvar:1 | ||||
chr11:68271891-68272134 | Common:2; Rare:103 | ||||
chr11:68460223-68460312 | Common:2; Rare:48 | ||||
chr11:68460601-68460767 | Common:3; Rare:61 | ||||
chr11:68903774-68903946 | Common:4; Rare:82; Clinvar (benign):6 | ||||
chr11:69640792-69641181 | Rare:84 | ||||
chr11:69675307-69675519 | Rare:56 | ||||
chr11:70398349-70398596 | Common:2; Rare:86 | ||||
chr11:70661783-70661904 | Rare:32 | ||||
chr11:70826674-70826912 | Rare:57 | ||||
chr11:70827189-70827374 | Common:1; Rare:25 | ||||
chr11:71448328-71448715 | Common:4; Rare:102; Clinvar:3; Clinvar (benign):1 | ||||
chr11:71452970-71453262 | Common:4; Rare:83 |