Variant report

Variant	rs10223188
Chromosome Location	chr5:89494000-89494001
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10037562	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10059737	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10805866	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11949043	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11952429	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28829709	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2950039	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2973380	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4404712	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4916787	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57707198	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6883979	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6886970	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7704328	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021142	chr5:89102893-89897826	Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv537804	chr5:89102893-89897826	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv917025	chr5:89208994-89855436	Enhancers Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv432750	chr5:89410113-90137144	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv882362	chr5:89437963-89604380	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv830391	chr5:89456582-89641195	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv432751	chr5:89457044-90090444	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89488600-89494000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr5:89488600-89494000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:89494000-89494600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:89494000-89495000	Enhancers	HUES6 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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