Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:61816134-61816290 | Rare:37 | ||||
chr11:61816587-61816611 | Rare:3 | ||||
chr11:61828045-61828360 | Common:1; Rare:75 | ||||
chr11:62612935-62613272 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
chr11:62646600-62646863 | Common:2; Rare:89 | ||||
chr11:62653279-62653412 | Common:1; Rare:36 | ||||
chr11:62665143-62665312 | Common:3; Rare:75 | ||||
chr11:62706261-62706421 | Common:2; Rare:76; Clinvar (benign):3 | ||||
chr11:62727455-62727702 | Rare:92 | ||||
chr11:62728412-62728538 | Common:2; Rare:73 | ||||
chr11:62787315-62787442 | Common:2; Rare:92 | ||||
chr11:62832004-62832291 | Common:1; Rare:104 | ||||
chr11:62855879-62856008 | Rare:56 | ||||
chr11:63986670-63986869 | Common:2; Rare:57 | ||||
chr11:64165935-64166180 | Common:1; Rare:68 |