Variant report

Variant rs10792768
Chromosome Location chr11:71256728-71256729
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:71232800-71259800 Weak transcription Brain Cingulate Gyrus brain
2 chr11:71252800-71257000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr11:71252800-71257000 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr11:71256000-71260000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr11:71256200-71256800 Enhancers iPS-18 Cell Line embryonic stem cell
6 chr11:71256400-71256800 Enhancers Lung lung
7 chr11:71256400-71256800 Flanking Active TSS HepG2 liver
8 chr11:71256400-71257000 Active TSS H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr11:71256400-71257000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr11:71256600-71256800 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr11:71256600-71256800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr11:71256600-71256800 Enhancers Fetal Intestine Small intestine
13 chr11:71256600-71256800 Enhancers Left Ventricle heart

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