Variant report

Variant	rs8032432
Chromosome Location	chr15:54528254-54528255
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10518760	0.86[ASN][1000 genomes]
rs11071065	0.92[CEU][hapmap]
rs11071066	0.92[CEU][hapmap]
rs11630366	0.88[CEU][hapmap]
rs11630766	0.95[CEU][hapmap]
rs11635437	0.92[CEU][hapmap]
rs11635678	0.87[EUR][1000 genomes]
rs11856476	0.85[ASN][1000 genomes]
rs12439702	0.96[CEU][hapmap]
rs12441013	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs12899415	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12899426	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12902112	0.95[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12902524	0.88[CEU][hapmap]
rs12903297	0.92[CEU][hapmap]
rs12903779	0.87[CEU][hapmap]
rs12906904	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12907862	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12908083	0.88[CEU][hapmap]
rs12912762	0.80[CEU][hapmap]
rs12914335	0.81[CEU][hapmap]
rs12914912	0.92[CEU][hapmap]
rs12916984	0.88[CEU][hapmap]
rs12917198	0.88[CEU][hapmap]
rs2414285	0.96[CEU][hapmap]
rs2414288	0.95[CEU][hapmap]
rs4144949	0.96[CEU][hapmap]
rs4517736	0.88[CEU][hapmap]
rs4774689	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4774691	0.92[CEU][hapmap]
rs4776215	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4776216	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4776219	0.83[CEU][hapmap]
rs4776220	0.88[CEU][hapmap]
rs4776222	0.96[CEU][hapmap]
rs5025252	0.88[CEU][hapmap]
rs6493669	0.96[CEU][hapmap]
rs6493670	0.96[CEU][hapmap]
rs7162346	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7172577	0.88[CEU][hapmap]
rs7183052	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7183952	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs719211	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8023723	0.88[EUR][1000 genomes]
rs8025731	0.86[ASN][1000 genomes]
rs8026128	0.84[CEU][hapmap]
rs8027105	0.87[EUR][1000 genomes]
rs8030298	0.89[EUR][1000 genomes]
rs8031083	0.81[CEU][hapmap]
rs8033291	0.91[EUR][1000 genomes]
rs8034428	0.92[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052235	chr15:53677524-54618723	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542388	chr15:53677524-54618723	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1043666	chr15:54415970-54548495	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1043823	chr15:54468477-54532985	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54516800-54529000	Weak transcription	Fetal Lung	lung
2	chr15:54519000-54554400	Weak transcription	Aorta	Aorta
3	chr15:54519400-54549600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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