Variant report

Variant	rs60781553
Chromosome Location	chr8:63713552-63713553
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10086439	1.00[ASN][1000 genomes]
rs11986003	1.00[ASN][1000 genomes]
rs11988844	1.00[ASN][1000 genomes]
rs11990729	1.00[ASN][1000 genomes]
rs11993139	1.00[ASN][1000 genomes]
rs11994250	1.00[ASN][1000 genomes]
rs11997540	1.00[ASN][1000 genomes]
rs13439148	1.00[ASN][1000 genomes]
rs13439149	1.00[ASN][1000 genomes]
rs16929324	1.00[ASN][1000 genomes]
rs16929355	1.00[ASN][1000 genomes]
rs16929366	1.00[ASN][1000 genomes]
rs16929379	1.00[ASN][1000 genomes]
rs16929380	1.00[ASN][1000 genomes]
rs16929392	1.00[ASN][1000 genomes]
rs16929407	1.00[ASN][1000 genomes]
rs16929409	1.00[ASN][1000 genomes]
rs16929424	1.00[ASN][1000 genomes]
rs16929428	1.00[ASN][1000 genomes]
rs17840589	1.00[ASN][1000 genomes]
rs2127562	1.00[ASN][1000 genomes]
rs2127563	1.00[ASN][1000 genomes]
rs2127564	1.00[ASN][1000 genomes]
rs28608015	1.00[ASN][1000 genomes]
rs4562311	1.00[ASN][1000 genomes]
rs56083055	1.00[ASN][1000 genomes]
rs59113187	1.00[ASN][1000 genomes]
rs60508325	1.00[ASN][1000 genomes]
rs61408776	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6472043	1.00[ASN][1000 genomes]
rs6997907	1.00[ASN][1000 genomes]
rs7007446	1.00[ASN][1000 genomes]
rs7016043	1.00[ASN][1000 genomes]
rs73682630	1.00[ASN][1000 genomes]
rs73682631	1.00[ASN][1000 genomes]
rs73683352	1.00[ASN][1000 genomes]
rs73685419	1.00[ASN][1000 genomes]
rs7820024	1.00[ASN][1000 genomes]
rs961828	1.00[ASN][1000 genomes]
rs9969432	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831341	chr8:63658694-63852213	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1033527	chr8:63673915-64073735	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv521804	chr8:63705238-63758070	Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv890961	chr8:63708519-63773787	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv890962	chr8:63708519-63812686	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv3342180	chr8:63709447-63734873	Active TSS Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
8	esv3341182	chr8:63712447-63734873	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63713000-63713600	Active TSS	HUES6 Cell Line	embryonic stem cell

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