Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113073111-113073249 | Common:1; Rare:55 | ||||
chr1:113759458-113759630 | Common:2; Rare:53 | ||||
chr1:113904779-113905375 | Common:6; Rare:173; Clinvar (benign):2 | ||||
chr1:113929549-113929665 | Common:1; Rare:33 | ||||
chr1:114511197-114511414 | Common:4; Rare:84 | ||||
chr1:114581565-114581810 | Common:1; Rare:115 | ||||
chr1:114716659-114716985 | Common:4; Rare:124; Clinvar:5; Clinvar (benign):3 | ||||
chr1:115337659-115337856 | Rare:46 | ||||
chr1:115641638-115642006 | Common:5; Rare:104; Clinvar:1; Clinvar (benign):2 | ||||
chr1:116398762-116399084 | Common:1; Rare:69 | ||||
chr1:116400867-116401213 | Rare:72 | ||||
chr1:117060062-117060349 | Common:6; Rare:71 | ||||
chr1:117121526-117121644 | Rare:23 | ||||
chr1:117366568-117366956 | Common:1; Rare:110 | ||||
chr1:117367297-117367516 | Common:5; Rare:81 |