Variant report

Variant rs11226828
Chromosome Location chr11:105568411-105568412
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:105561400-105586200 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr11:105564800-105569400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr11:105564800-105569600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr11:105566600-105569600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr11:105567000-105596600 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr11:105567800-105568600 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr11:105568000-105568600 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr11:105568000-105568600 Enhancers H9 Cell Line embryonic stem cell
9 chr11:105568000-105568600 Enhancers HUES48 Cell Line embryonic stem cell
10 chr11:105568000-105568600 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr11:105568200-105568600 Enhancers Brain Hippocampus Middle brain
12 chr11:105568200-105570200 Enhancers Brain Inferior Temporal Lobe brain
13 chr11:105568200-105571600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
14 chr11:105568200-105572000 Enhancers Brain Substantia Nigra brain
15 chr11:105568400-105570400 Enhancers Cortex derived primary cultured neurospheres brain

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