Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116400762-116400888 | Common:1; Rare:29; Clinvar (pathogenic):1 | ||||
chr1:116400897-116401267 | Rare:78 | ||||
chr1:116667672-116667845 | Common:1; Rare:65 | ||||
chr1:116754347-116754531 | Rare:50 | ||||
chr1:116909823-116910187 | Common:1; Rare:111 | ||||
chr1:117060037-117060360 | Common:7; Rare:86 | ||||
chr1:117367308-117367559 | Common:5; Rare:90 | ||||
chr1:117368205-117368485 | Rare:73 | ||||
chr1:117605765-117606057 | Rare:87 | ||||
chr1:117929560-117929800 | Common:2; Rare:70 | ||||
chr1:119140612-119140776 | Common:1; Rare:59 | ||||
chr1:119648133-119648367 | Common:3; Rare:80 | ||||
chr1:120069527-120070042 | Common:7; Rare:94 | ||||
chr1:120176306-120176593 | Rare:59 | ||||
chr1:120914083-120914197 | Rare:12 |