Variant report

Variant	rs9416306
Chromosome Location	chr10:56071606-56071607
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10430538	1.00[JPT][hapmap]
rs10763098	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10825296	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10825299	0.82[CHB][hapmap]
rs10825325	0.82[JPT][hapmap]
rs11004217	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs11004279	0.82[JPT][hapmap]
rs1219862	0.82[JPT][hapmap]
rs12358060	0.82[CHB][hapmap]
rs12358062	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12778129	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs1342280	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1418367	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1612430	0.82[JPT][hapmap]
rs16906104	0.82[JPT][hapmap]
rs17725837	0.82[CHB][hapmap]
rs1774653	0.82[JPT][hapmap]
rs2384437	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2384442	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2795918	0.82[JPT][hapmap]
rs2891514	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4287260	0.82[JPT][hapmap]
rs4481936	0.82[JPT][hapmap]
rs4483501	0.82[JPT][hapmap]
rs4935515	0.82[JPT][hapmap]
rs4935516	0.82[JPT][hapmap]
rs4935519	0.82[JPT][hapmap]
rs7092253	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]
rs7098778	0.85[JPT][hapmap]
rs7350458	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7911706	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs7915662	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7917641	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7918858	0.82[JPT][hapmap]
rs857369	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap]
rs857376	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs920526	0.96[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948730	chr10:55845301-56093271	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1054364	chr10:55925471-56196447	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv540633	chr10:55925471-56196447	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2753511	chr10:56022197-56153636	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv6698	chr10:56030123-56074572	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1044020	chr10:56038546-56224736	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv540634	chr10:56038546-56224736	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv1048014	chr10:56053413-56104109	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv831879	chr10:56059973-56210729	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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