Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:34357998-34358305 | Common:2; Rare:80 | ||||
chr11:34438776-34439003 | Common:2; Rare:75; Clinvar (benign):1 | ||||
chr11:34916318-34916676 | Common:10; Rare:145; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr11:35139008-35139339 | Common:1; Rare:89 | ||||
chr11:35525586-35525816 | Rare:55 | ||||
chr11:35943958-35944133 | Common:2; Rare:62 | ||||
chr11:36510236-36510374 | Rare:39 | ||||
chr11:43358813-43358983 | Rare:82 | ||||
chr11:44066189-44066540 | Common:3; Rare:89 | ||||
chr11:45847204-45847491 | Common:2; Rare:114 | ||||
chr11:46277824-46278066 | Rare:63 | ||||
chr11:46345353-46345487 | Rare:49 | ||||
chr11:46617186-46617579 | Common:5; Rare:113 | ||||
chr11:46700555-46700818 | Common:1; Rare:68 | ||||
chr11:46846207-46846421 | Common:1; Rare:63 |