Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:75562194-75562292 | Common:1; Rare:28; Clinvar (benign):1 | ||||
chr11:76381075-76381408 | Common:4; Rare:114 | ||||
chr11:76444647-76445085 | Common:1; Rare:104 | ||||
chr11:76783048-76783379 | Common:10; Rare:112 | ||||
chr11:77589886-77589953 | Rare:18 | ||||
chr11:77637739-77637858 | Common:1; Rare:48 | ||||
chr11:77820848-77821164 | Common:1; Rare:88 | ||||
chr11:78139587-78139806 | Common:3; Rare:87; Clinvar:2 | ||||
chr11:78188588-78188953 | Common:3; Rare:114 | ||||
chr11:78417773-78417994 | Common:1; Rare:88 | ||||
chr11:78574773-78574970 | Common:2; Rare:78; Clinvar (benign):1 | ||||
chr11:83071797-83072124 | Common:4; Rare:91 | ||||
chr11:83193608-83193804 | Common:1; Rare:92 | ||||
chr11:83285906-83286131 | Common:3; Rare:104 | ||||
chr11:83286333-83286479 | Rare:34 |