Variant report

Variant rs36112669
Chromosome Location chr5:178956605-178956606
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:178951000-178957000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr5:178954600-178956800 Weak transcription Primary monocytes fromperipheralblood blood
3 chr5:178954600-178957200 Weak transcription Spleen Spleen
4 chr5:178954800-178957400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr5:178955000-178956800 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr5:178956400-178958800 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr5:178956600-178956800 Genic enhancers Primary hematopoietic stem cells short term culture blood
8 chr5:178956600-178956800 Enhancers Adipose Nuclei Adipose
9 chr5:178956600-178956800 Enhancers Duodenum Mucosa Duodenum
10 chr5:178956600-178957000 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr5:178956600-178957000 Enhancers Brain Inferior Temporal Lobe brain
12 chr5:178956600-178957000 Enhancers Colon Smooth Muscle Colon
13 chr5:178956600-178957000 Enhancers Thymus Thymus
14 chr5:178956600-178957400 Flanking Active TSS Primary hematopoietic stem cells blood
15 chr5:178956600-178957400 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr5:178956600-178957800 Active TSS iPS-15b Cell Line embryonic stem cell
17 chr5:178956600-178958200 Active TSS GM12878-XiMat blood
18 chr5:178956600-178958800 Flanking Active TSS Dnd41 blood

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