Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:87345477-87345701 | Common:4; Rare:71 | ||||
chr7:87876294-87876552 | Common:1; Rare:116 | ||||
chr7:92528484-92528807 | Common:3; Rare:95; Clinvar (benign):2 | ||||
chr7:94656134-94656374 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
chr7:99325781-99325941 | Common:1; Rare:65 | ||||
chr7:99408546-99409018 | Common:3; Rare:136 | ||||
chr7:100088843-100088984 | Common:1; Rare:48 | ||||
chr7:100101329-100101648 | Common:1; Rare:120 | ||||
chr7:100119346-100119728 | Rare:117 | ||||
chr7:102478886-102479183 | Common:7; Rare:121 | ||||
chr7:106112234-106112490 | Common:3; Rare:84 | ||||
chr7:107563897-107563971 | Common:1; Rare:43; Clinvar (benign):1 | ||||
chr7:107744053-107744159 | Rare:36 | ||||
chr7:108569584-108569931 | Common:1; Rare:120 | ||||
chr7:116499514-116499796 | Common:3; Rare:95 |