Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:88337670-88337980 | Common:6; Rare:136; Clinvar:6; Clinvar (benign):3 | ||||
chr11:89491129-89491355 | Common:3; Rare:89 | ||||
chr11:90134495-90134705 | Common:1; Rare:51 | ||||
chr11:90223023-90223263 | Common:2; Rare:92 | ||||
chr11:93197406-93197593 | Common:1; Rare:43 | ||||
chr11:93197856-93198185 | Common:3; Rare:96 | ||||
chr11:93543389-93543520 | Common:2; Rare:27 | ||||
chr11:93661471-93661738 | Common:1; Rare:75 | ||||
chr11:93741421-93741745 | Common:5; Rare:124 | ||||
chr11:93783948-93784388 | Common:6; Rare:116 | ||||
chr11:94128726-94128980 | Common:2; Rare:96 | ||||
chr11:94493832-94494020 | Common:3; Rare:52; Clinvar (benign):1 | ||||
chr11:94544260-94544710 | Common:2; Rare:193 | ||||
chr11:94706088-94706488 | Common:7; Rare:92 | ||||
chr11:94768190-94768445 | Common:2; Rare:78 |