Variant report

Variant rs4841647
Chromosome Location chr8:11801757-11801758
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11800200-11804600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr8:11800400-11804200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr8:11800800-11804400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr8:11800800-11807200 Weak transcription Right Atrium heart
5 chr8:11801000-11801800 Enhancers Dnd41 blood
6 chr8:11801200-11801800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr8:11801200-11801800 Bivalent Enhancer Stomach Smooth Muscle stomach
8 chr8:11801400-11801800 Bivalent Enhancer Primary B cells from peripheral blood blood
9 chr8:11801400-11801800 Enhancers Primary T helper memory cells from peripheral blood 2 blood
10 chr8:11801400-11801800 Flanking Bivalent TSS/Enh Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr8:11801400-11801800 Active TSS Brain Angular Gyrus brain
12 chr8:11801400-11801800 Flanking Active TSS Brain Hippocampus Middle brain
13 chr8:11801400-11801800 Flanking Active TSS Brain Substantia Nigra brain
14 chr8:11801400-11801800 Bivalent Enhancer NHDF-Ad bronchial
15 chr8:11801400-11801800 Bivalent Enhancer NHLF lung
16 chr8:11801600-11801800 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr8:11801600-11801800 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr8:11801600-11801800 Active TSS Liver Liver
19 chr8:11801600-11801800 Active TSS Duodenum Mucosa Duodenum
20 chr8:11801600-11806800 Weak transcription Fetal Heart heart

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