Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113812264-113812581 | Common:2; Rare:125 | ||||
chr1:113905026-113905357 | Common:3; Rare:90 | ||||
chr1:114669991-114670196 | Rare:68 | ||||
chr1:114716731-114716929 | Common:1; Rare:86; Clinvar:5; Clinvar (benign):1 | ||||
chr1:115089446-115089622 | Common:3; Rare:71 | ||||
chr1:116398522-116399072 | Common:1; Rare:111 | ||||
chr1:116400597-116400988 | Common:1; Rare:88; Clinvar (pathogenic):1 | ||||
chr1:116754351-116754485 | Rare:39 | ||||
chr1:117367317-117367490 | Common:4; Rare:60 | ||||
chr1:117368205-117368387 | Rare:43 | ||||
chr1:117605783-117606048 | Rare:74 | ||||
chr1:117929555-117929795 | Common:1; Rare:72 | ||||
chr1:119140639-119140767 | Rare:38 | ||||
chr1:121184923-121185077 | Rare:51 | ||||
chr1:145823927-145824238 | Rare:107 |