Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:61392527-61392651 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429270-61429349 | Common:2; Rare:29 | ||||
chr11:61429892-61430169 | Common:1; Rare:121; Clinvar:3; Clinvar (benign):5 | ||||
chr11:61792564-61792948 | Common:5; Rare:106 | ||||
chr11:61816764-61816866 | Rare:32 | ||||
chr11:61827822-61828148 | Common:1; Rare:49 | ||||
chr11:61917361-61917658 | Common:2; Rare:103 | ||||
chr11:61967158-61967300 | Common:1; Rare:44 | ||||
chr11:61967311-61967571 | Common:1; Rare:97; Clinvar:1 | ||||
chr11:61967580-61967806 | Common:2; Rare:87; Clinvar:3 | ||||
chr11:62123808-62124127 | Common:6; Rare:79 | ||||
chr11:62337400-62337510 | Common:2; Rare:31 | ||||
chr11:62545564-62546020 | Common:1; Rare:102 | ||||
chr11:62546660-62547046 | Common:1; Rare:117 | ||||
chr11:62591478-62591837 | Rare:122 |