Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:106284978-106285276 | Common:2; Rare:112 | ||||
chr7:107563888-107564022 | Common:2; Rare:79; Clinvar (benign):3 | ||||
chr7:107580144-107580296 | Common:2; Rare:61 | ||||
chr7:107744062-107744171 | Rare:34 | ||||
chr7:108526095-108526475 | Common:5; Rare:116 | ||||
chr7:108569592-108569992 | Common:2; Rare:143 | ||||
chr7:112206318-112206725 | Common:2; Rare:132 | ||||
chr7:112450176-112450462 | Common:6; Rare:85 | ||||
chr7:114086197-114086520 | Common:2; Rare:120 | ||||
chr7:116210402-116210601 | Common:3; Rare:53 | ||||
chr7:116499509-116499790 | Common:3; Rare:95 | ||||
chr7:118184001-118184203 | Common:1; Rare:78 | ||||
chr7:120950502-120950839 | Common:2; Rare:105 | ||||
chr7:120988687-120989043 | Common:1; Rare:62 | ||||
chr7:122144215-122144440 | Common:1; Rare:49 |