Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:78574823-78574964 | Common:2; Rare:49; Clinvar (benign):1 | ||||
chr11:83071794-83072124 | Common:4; Rare:91 | ||||
chr11:83193621-83193759 | Common:1; Rare:63 | ||||
chr11:83285925-83286117 | Common:3; Rare:90 | ||||
chr11:83286333-83286478 | Rare:34 | ||||
chr11:85628339-85628664 | Common:6; Rare:109 | ||||
chr11:85647872-85648020 | Rare:35; Clinvar:2 | ||||
chr11:86069088-86069184 | Rare:36 | ||||
chr11:86245047-86245332 | Common:1; Rare:129 | ||||
chr11:86302093-86302346 | Common:3; Rare:49 | ||||
chr11:87037762-87038057 | Common:3; Rare:139 | ||||
chr11:87317530-87317749 | Rare:37 | ||||
chr11:88337661-88337845 | Common:4; Rare:96; Clinvar:6; Clinvar (benign):3 | ||||
chr11:90223015-90223139 | Common:1; Rare:48 | ||||
chr11:93661522-93661733 | Common:1; Rare:60 |