Variant report

Variant rs2759690
Chromosome Location chr13:53712903-53712904
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr13:53711200-53717200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr13:53711800-53713200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr13:53712000-53713000 Enhancers Fetal Lung lung
7 chr13:53712200-53713200 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr13:53712200-53713200 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr13:53712400-53713800 Enhancers Fetal Muscle Leg muscle
10 chr13:53712600-53713000 Enhancers Fetal Heart heart
11 chr13:53712600-53713200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr13:53712600-53713200 Flanking Active TSS Adipose Nuclei Adipose
13 chr13:53712600-53713600 Enhancers Brain Germinal Matrix brain
14 chr13:53712600-53713600 Enhancers Brain Hippocampus Middle brain
15 chr13:53712800-53713000 Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr13:53712800-53713000 Flanking Bivalent TSS/Enh Fetal Muscle Trunk muscle
17 chr13:53712800-53713200 Active TSS K562 blood
18 chr13:53712800-53713400 Enhancers Fetal Brain Male brain

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