Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117367297-117367538 | Common:5; Rare:88 | ||||
chr1:117367638-117368092 | Common:1; Rare:94 | ||||
chr1:117368098-117368478 | Rare:104 | ||||
chr1:117929560-117929916 | Common:4; Rare:111 | ||||
chr1:119140578-119140815 | Common:1; Rare:87; Clinvar (pathogenic):1 | ||||
chr1:119648096-119648405 | Common:3; Rare:98 | ||||
chr1:120176054-120176565 | Common:1; Rare:98 | ||||
chr1:121184795-121185085 | Common:1; Rare:98 | ||||
chr1:145773451-145773864 | Common:4; Rare:70 | ||||
chr1:145774260-145774315 | Rare:9 | ||||
chr1:145823787-145823905 | Rare:45 | ||||
chr1:145823907-145824393 | Rare:155 | ||||
chr1:145836374-145836583 | Rare:57 | ||||
chr1:145845352-145845647 | Common:4; Rare:75 | ||||
chr1:145858962-145859179 | Rare:62 |