Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:95089715-95089927 | Common:3; Rare:91 | ||||
chr11:95789474-95789846 | Common:3; Rare:171 | ||||
chr11:95790350-95790633 | Common:1; Rare:107 | ||||
chr11:95923944-95924158 | Common:1; Rare:94; Clinvar (benign):2 | ||||
chr11:96342758-96343061 | Rare:47 | ||||
chr11:96389862-96390052 | Common:1; Rare:77 | ||||
chr11:101914858-101915373 | Common:8; Rare:153 | ||||
chr11:102110209-102110470 | Common:1; Rare:102 | ||||
chr11:102347111-102347463 | Common:5; Rare:101 | ||||
chr11:102448848-102449145 | Rare:66 | ||||
chr11:102452612-102452899 | Common:1; Rare:91 | ||||
chr11:102838587-102838929 | Common:4; Rare:88; Clinvar (benign):1 | ||||
chr11:103109661-103109728 | Rare:14 | ||||
chr11:106077326-106077711 | Common:2; Rare:115 | ||||
chr11:108008820-108008971 | Rare:46 |