Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114716665-114716862 | Common:1; Rare:79; Clinvar:4; Clinvar (benign):3 | ||||
chr1:114757925-114758190 | Common:3; Rare:83 | ||||
chr1:114780569-114780787 | Common:1; Rare:83 | ||||
chr1:115089455-115089622 | Common:3; Rare:64 | ||||
chr1:116373114-116373349 | Rare:78 | ||||
chr1:116909580-116910202 | Common:4; Rare:185 | ||||
chr1:117121726-117122028 | Common:1; Rare:90 | ||||
chr1:117929556-117929787 | Common:1; Rare:70 | ||||
chr1:119140632-119140724 | Rare:28 | ||||
chr1:119648133-119648364 | Common:3; Rare:80 | ||||
chr1:120176306-120176647 | Common:1; Rare:63 | ||||
chr1:121184754-121184997 | Common:1; Rare:83 | ||||
chr1:145823933-145824260 | Rare:115 | ||||
chr1:145845619-145845654 | Common:1; Rare:16 | ||||
chr1:145858996-145859175 | Rare:51 |