Variant report

Variant	rs180965509
Chromosome Location	chr3:155751585-155751586
allele	A/G
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	nsv592084	chr3:155751484-155830578	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155750800-155751600	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr3:155751000-155751600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr3:155751000-155751600	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr3:155751000-155751600	Enhancers	Brain Hippocampus Middle	brain
5	chr3:155751000-155751600	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr3:155751000-155751600	Enhancers	Brain Substantia Nigra	brain
7	chr3:155751200-155751600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr3:155751200-155751600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:155751400-155754400	Weak transcription	Brain Cingulate Gyrus	brain

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Input of quick search could be:

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

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