Variant report

Variant rs4895609
Chromosome Location chr6:143678135-143678136
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:143645000-143683200 Weak transcription Pancreas Pancrea
2 chr6:143673000-143708000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr6:143676400-143682600 Weak transcription Left Ventricle heart
4 chr6:143677800-143678600 Enhancers Fetal Stomach stomach
5 chr6:143678000-143678200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr6:143678000-143678400 Enhancers Liver Liver
7 chr6:143678000-143678400 Enhancers Ovary ovary
8 chr6:143678000-143679400 Enhancers Fetal Intestine Large intestine
9 chr6:143678000-143679400 Enhancers Fetal Lung lung
10 chr6:143678000-143679600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr6:143678000-143679600 Enhancers Adipose Nuclei Adipose
12 chr6:143678000-143679600 Enhancers Fetal Intestine Small intestine

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