Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65872723-65872937 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
chr11:65888426-65888587 | Common:1; Rare:62 | ||||
chr11:65900371-65900669 | Common:3; Rare:64 | ||||
chr11:65920035-65920105 | Rare:27 | ||||
chr11:65961547-65961733 | Rare:62 | ||||
chr11:66002134-66002818 | Common:4; Rare:188; Clinvar:3; Clinvar (benign):3 | ||||
chr11:66289086-66289427 | Common:1; Rare:85 | ||||
chr11:66371741-66371937 | Common:1; Rare:53 | ||||
chr11:66480239-66480452 | Common:1; Rare:57 | ||||
chr11:66616414-66616636 | Common:1; Rare:56 | ||||
chr11:66638393-66638725 | Common:3; Rare:146 | ||||
chr11:67303356-67303582 | Rare:58 | ||||
chr11:67353459-67353721 | Common:1; Rare:64 | ||||
chr11:67373596-67373848 | Rare:48 | ||||
chr11:67401774-67402075 | Common:3; Rare:113 |