Variant report

Variant	rs9466847
Chromosome Location	chr6:23585350-23585351
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs13437154	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9295588	1.00[AMR][1000 genomes]
rs9460892	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9460909	1.00[AMR][1000 genomes]
rs9466786	1.00[AMR][1000 genomes]
rs9466794	1.00[AMR][1000 genomes]
rs9466804	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9466808	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9466814	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9466817	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9466853	1.00[AMR][1000 genomes]
rs9466885	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422291	chr6:23466080-23600459	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1029930	chr6:23481989-24289948	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv830608	chr6:23558655-23644405	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	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	chr6:23583200-23585800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:23583800-23585400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:23584000-23585400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:23584000-23585400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr6:23584000-23585600	Enhancers	Fetal Intestine Large	intestine
6	chr6:23584200-23585400	Enhancers	Fetal Intestine Small	intestine
7	chr6:23584600-23585800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr6:23584800-23587400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:23585000-23586000	Enhancers	HepG2	liver
10	chr6:23585000-23587600	Weak transcription	Liver	Liver

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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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