Variant report

Variant rs6802139
Chromosome Location chr3:135627433-135627434
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:135625600-135628200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr3:135626000-135627800 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr3:135626200-135628200 Enhancers Placenta Amnion Placenta Amnion
4 chr3:135626400-135627600 Flanking Active TSS NHEK skin
5 chr3:135626400-135627800 Enhancers Placenta Placenta
6 chr3:135627000-135627600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr3:135627000-135627600 Enhancers Pancreas Pancrea
8 chr3:135627200-135627600 Enhancers Lung lung
9 chr3:135627200-135628000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr3:135627400-135627600 Enhancers Gastric stomach
11 chr3:135627400-135627800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr3:135627400-135627800 Enhancers Esophagus oesophagus
13 chr3:135627400-135628000 Enhancers HMEC breast
14 chr3:135627400-135629800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
15 chr3:135627400-135630200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr3:135627400-135632000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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