Variant report

Variant	rs17120966
Chromosome Location	chr14:85748085-85748086
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11845784	1.00[AMR][1000 genomes]
rs58628367	1.00[AMR][1000 genomes]
rs61594569	1.00[AMR][1000 genomes]
rs74068328	1.00[EUR][1000 genomes]
rs74068340	1.00[EUR][1000 genomes]
rs74070038	1.00[EUR][1000 genomes]

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	esv2422273	chr14:85703149-85767292	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85743800-85750200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr14:85746000-85748600	Enhancers	HUVEC	blood vessel
3	chr14:85747600-85748400	Enhancers	Primary hematopoietic stem cells	blood
4	chr14:85747800-85748200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:85747800-85748600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:85747800-85748600	Enhancers	Fetal Kidney	kidney
7	chr14:85747800-85748800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr14:85748000-85748600	Enhancers	Primary hematopoietic stem cells short term culture	blood

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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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