Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:70114117-70114393 | Common:3; Rare:99 | ||||
chr16:70523539-70523837 | Common:3; Rare:92 | ||||
chr16:71564926-71564984 | Rare:21 | ||||
chr16:71626157-71626226 | Common:1; Rare:24 | ||||
chr16:71808766-71808826 | Rare:40 | ||||
chr16:71808828-71809345 | Common:4; Rare:170 | ||||
chr16:71845879-71846023 | Common:2; Rare:49 | ||||
chr16:71895318-71895568 | Common:2; Rare:92 | ||||
chr16:72008541-72008760 | Common:3; Rare:69; Clinvar (benign):1 | ||||
chr16:72093584-72093934 | Rare:87 | ||||
chr16:74296696-74296916 | Rare:90 | ||||
chr16:74472389-74472691 | Common:2; Rare:73 | ||||
chr16:75206617-75206872 | Common:2; Rare:73 | ||||
chr16:75207013-75207583 | Common:4; Rare:150 | ||||
chr16:75218697-75219187 | Common:4; Rare:167 |