Variant report

Variant rs6561706
Chromosome Location chr13:53712380-53712381
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:53708800-53715200 Weak transcription H1 Cell Line embryonic stem cell
2 chr13:53710000-53715600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr13:53710200-53713000 Enhancers Fetal Stomach stomach
4 chr13:53710600-53712800 Enhancers Primary neutrophils fromperipheralblood blood
5 chr13:53711200-53717200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr13:53711400-53712600 Enhancers Adipose Nuclei Adipose
7 chr13:53711800-53713200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr13:53712000-53712400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr13:53712000-53712800 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr13:53712000-53712800 Enhancers Duodenum Smooth Muscle Duodenum
11 chr13:53712000-53713000 Enhancers Fetal Lung lung
12 chr13:53712200-53712600 Enhancers NH-A brain
13 chr13:53712200-53712600 Enhancers NHLF lung
14 chr13:53712200-53712800 Enhancers Fetal Intestine Small intestine
15 chr13:53712200-53713200 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr13:53712200-53713200 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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