Variant report

Variant	rs191404416
Chromosome Location	chr2:180275720-180275721
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv962512	chr2:180271870-180286262	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180275200-180275800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:180275400-180275800	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr2:180275400-180275800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
4	chr2:180275400-180276000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
5	chr2:180275400-180276000	Enhancers	Primary T cells fromperipheralblood	blood
6	chr2:180275400-180276000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr2:180275600-180275800	Enhancers	Brain Anterior Caudate	brain
8	chr2:180275600-180275800	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr2:180275600-180276000	Enhancers	Adipose Nuclei	Adipose
10	chr2:180275600-180277200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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