Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:107580157-107580286 | Common:2; Rare:52 | ||||
chr7:107744053-107744164 | Rare:37 | ||||
chr7:108526113-108526424 | Common:5; Rare:96 | ||||
chr7:108569555-108570040 | Common:3; Rare:173 | ||||
chr7:112206269-112206719 | Common:3; Rare:137 | ||||
chr7:112450285-112450599 | Common:4; Rare:94 | ||||
chr7:114086278-114086545 | Common:1; Rare:108 | ||||
chr7:116499499-116499821 | Common:3; Rare:111 | ||||
chr7:116672231-116672473 | Common:1; Rare:56; Clinvar:2 | ||||
chr7:116953165-116953505 | Common:3; Rare:71 | ||||
chr7:117479700-117480007 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
chr7:118183957-118184217 | Common:2; Rare:103 | ||||
chr7:118214548-118214664 | Common:2; Rare:37 | ||||
chr7:120950500-120950825 | Common:2; Rare:104 | ||||
chr7:120988664-120988740 | Rare:21 |