Variant report

Variant rs116695275
Chromosome Location chr11:71351996-71351997
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:71350400-71352000 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
2 chr11:71350800-71354400 Weak transcription Esophagus oesophagus
3 chr11:71351200-71353400 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr11:71351800-71352000 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr11:71351800-71352000 Enhancers Fetal Intestine Large intestine
6 chr11:71351800-71352000 Flanking Active TSS Fetal Intestine Small intestine
7 chr11:71351800-71352200 Flanking Active TSS H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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