Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112956165-112956467 | Common:5; Rare:130; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073095-113073221 | Common:1; Rare:45 | ||||
chr1:113812241-113812630 | Common:3; Rare:155 | ||||
chr1:113871699-113871775 | Rare:15 | ||||
chr1:113904824-113905381 | Common:6; Rare:167; Clinvar (benign):1 | ||||
chr1:114581584-114581818 | Rare:104 | ||||
chr1:114670047-114670184 | Rare:40 | ||||
chr1:114716722-114716860 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):1 | ||||
chr1:114757942-114758118 | Common:3; Rare:55 | ||||
chr1:114780547-114780805 | Common:1; Rare:98 | ||||
chr1:117059911-117060360 | Common:7; Rare:114 | ||||
chr1:117605773-117606053 | Rare:81 | ||||
chr1:117929568-117929841 | Common:4; Rare:83 | ||||
chr1:119140634-119140776 | Common:1; Rare:47 | ||||
chr1:120176383-120176614 | Common:1; Rare:51 |