Variant report

Variant	rs9645781
Chromosome Location	chr12:86993989-86993990
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10047529	1.00[CHB][hapmap];0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10047643	1.00[CHB][hapmap];0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10160933	1.00[CHB][hapmap]
rs10735253	1.00[CHB][hapmap];0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10745428	1.00[CHB][hapmap]
rs10745429	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10776982	1.00[CHB][hapmap]
rs10776985	1.00[CHB][hapmap]
rs11609178	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs11609218	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs11609775	0.84[EUR][1000 genomes]
rs11609819	0.84[EUR][1000 genomes]
rs11610166	1.00[CHB][hapmap];0.92[AFR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11610247	0.91[AFR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11610801	0.93[AFR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11611942	0.84[EUR][1000 genomes]
rs11613065	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11614366	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11616058	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs11830847	1.00[CHB][hapmap];0.93[AFR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11833815	1.00[CHB][hapmap];0.84[AFR][1000 genomes]
rs11835122	1.00[CHB][hapmap];0.89[AFR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11836942	1.00[CHB][hapmap];0.89[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs11837474	1.00[CHB][hapmap]
rs12306070	1.00[CHB][hapmap]
rs12371750	1.00[CHB][hapmap]
rs17014083	1.00[CHB][hapmap];0.87[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs2042869	1.00[CHB][hapmap];0.86[AFR][1000 genomes]
rs2195229	1.00[CEU][hapmap]
rs2217233	1.00[CHB][hapmap];0.87[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs34603963	0.90[AFR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4280066	1.00[CHB][hapmap]
rs4309212	1.00[CHB][hapmap]
rs4309213	1.00[CHB][hapmap]
rs4359271	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4374001	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4427624	1.00[CHB][hapmap]
rs4465426	1.00[CHB][hapmap]
rs4508266	1.00[CHB][hapmap];0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs5027506	1.00[CHB][hapmap]
rs55860954	0.91[AFR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs56948187	0.93[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs58920773	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs59556648	0.84[AFR][1000 genomes]
rs6538047	1.00[CHB][hapmap]
rs6538048	1.00[CHB][hapmap]
rs7134480	1.00[CHB][hapmap]
rs7308935	1.00[CHB][hapmap];0.89[AFR][1000 genomes]
rs7485159	0.84[EUR][1000 genomes]
rs7957182	0.90[ASN][1000 genomes]
rs7968612	1.00[CHB][hapmap];0.85[AFR][1000 genomes]
rs9645772	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754127	chr12:86723232-87576932	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv899395	chr12:86813367-87177972	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv916862	chr12:86837694-87718558	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv899396	chr12:86863041-87276957	ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv899397	chr12:86863041-87636831	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv899398	chr12:86880442-87051310	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv899399	chr12:86880442-87177972	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv559690	chr12:86929340-87020377	Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv916604	chr12:86966256-87275268	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1049580	chr12:86966497-87354132	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 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
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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