Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:104207972-104208080 | Common:1; Rare:48 | ||||
chr7:105013595-105013719 | Common:1; Rare:41 | ||||
chr7:105014052-105014274 | Common:3; Rare:87 | ||||
chr7:105532055-105532225 | Common:2; Rare:46 | ||||
chr7:105876481-105876818 | Common:6; Rare:99 | ||||
chr7:106284890-106285476 | Common:6; Rare:210 | ||||
chr7:106285539-106285583 | Rare:11 | ||||
chr7:107563888-107564026 | Common:2; Rare:83; Clinvar (benign):4 | ||||
chr7:107580168-107580306 | Common:2; Rare:53 | ||||
chr7:107744062-107744171 | Rare:34 | ||||
chr7:108003116-108003244 | Rare:38 | ||||
chr7:108569557-108569958 | Common:2; Rare:149 | ||||
chr7:112206384-112206744 | Common:1; Rare:129 | ||||
chr7:112939753-112940038 | Common:4; Rare:93 | ||||
chr7:116499521-116499790 | Common:3; Rare:92 |