Variant report

Variant rs554583279
Chromosome Location chr11:71351710-71351711
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:71350400-71351800 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
2 chr11:71350400-71351800 Active TSS Fetal Intestine Large intestine
3 chr11:71350400-71351800 Active TSS Fetal Intestine Small intestine
4 chr11:71350400-71352000 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
5 chr11:71350600-71351800 Active TSS H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr11:71350800-71354400 Weak transcription Esophagus oesophagus
7 chr11:71351200-71353400 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr11:71351400-71351800 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
9 chr11:71351400-71351800 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr11:71351400-71351800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr11:71351400-71351800 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
12 chr11:71351600-71351800 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell

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