Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111739350-111739540 | Common:1; Rare:50 | ||||
chr1:111755497-111755706 | Common:3; Rare:66 | ||||
chr1:112396000-112396267 | Common:1; Rare:84 | ||||
chr1:112619093-112619242 | Rare:55 | ||||
chr1:112619634-112619877 | Common:2; Rare:86 | ||||
chr1:112707080-112707227 | Rare:49 | ||||
chr1:112956150-112956659 | Common:6; Rare:169; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073095-113073247 | Common:1; Rare:58 | ||||
chr1:113390193-113390497 | Common:1; Rare:75 | ||||
chr1:113812260-113812608 | Common:2; Rare:135 | ||||
chr1:113904824-113905385 | Common:7; Rare:168; Clinvar (benign):1 | ||||
chr1:113929503-113929849 | Common:4; Rare:93 | ||||
chr1:114511100-114511384 | Common:3; Rare:136 | ||||
chr1:114581565-114581846 | Common:1; Rare:123 | ||||
chr1:114716733-114716862 | Common:1; Rare:58; Clinvar:4; Clinvar (benign):1 |