Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113759471-113759572 | Common:1; Rare:29 | ||||
chr1:113812260-113812383 | Common:2; Rare:55 | ||||
chr1:113904785-113905425 | Common:7; Rare:185; Clinvar (benign):1 | ||||
chr1:114716713-114716872 | Common:1; Rare:72; Clinvar:4; Clinvar (benign):1 | ||||
chr1:114757933-114758106 | Common:3; Rare:57 | ||||
chr1:114780547-114780806 | Common:1; Rare:98 | ||||
chr1:116373093-116373340 | Rare:83 | ||||
chr1:116400738-116400957 | Common:1; Rare:48; Clinvar (pathogenic):1 | ||||
chr1:117060037-117060359 | Common:7; Rare:86 | ||||
chr1:117929560-117929811 | Common:4; Rare:75 | ||||
chr1:119140640-119140767 | Rare:38 | ||||
chr1:119648126-119648405 | Common:3; Rare:88 | ||||
chr1:120176350-120176614 | Common:1; Rare:55 | ||||
chr1:120723758-120723949 | Rare:7 | ||||
chr1:120914087-120914192 | Rare:10 |