Variant report

Variant	rs7169339
Chromosome Location	chr15:54571441-54571442
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10851563	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10851564	0.85[ASN][1000 genomes]
rs11071065	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11071066	0.98[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11630366	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11630766	0.92[EUR][1000 genomes]
rs11635242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11635678	0.83[EUR][1000 genomes]
rs11638408	0.89[EUR][1000 genomes]
rs11638986	0.89[EUR][1000 genomes]
rs12441013	0.84[EUR][1000 genomes]
rs12900325	0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12902524	0.89[EUR][1000 genomes]
rs12903297	0.95[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12903779	0.88[EUR][1000 genomes]
rs12908083	0.89[EUR][1000 genomes]
rs12912246	0.89[EUR][1000 genomes]
rs12913239	0.89[EUR][1000 genomes]
rs12914912	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12915061	0.89[EUR][1000 genomes]
rs12916984	0.89[EUR][1000 genomes]
rs12917198	0.89[EUR][1000 genomes]
rs12917364	0.89[EUR][1000 genomes]
rs2414285	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2414288	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2414292	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2414294	0.82[EUR][1000 genomes]
rs4517736	0.89[EUR][1000 genomes]
rs4569201	0.83[AMR][1000 genomes]
rs4774691	0.97[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4776219	0.92[AFR][1000 genomes]
rs4776220	0.90[EUR][1000 genomes]
rs4776222	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5025252	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5027653	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58301914	0.96[EUR][1000 genomes]
rs6493669	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6493670	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6493674	0.82[EUR][1000 genomes]
rs7170994	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7172577	0.89[EUR][1000 genomes]
rs7176603	0.81[ASN][1000 genomes]
rs8023723	0.83[EUR][1000 genomes]
rs8027105	0.83[EUR][1000 genomes]
rs8030298	0.82[EUR][1000 genomes]
rs8030563	0.83[EUR][1000 genomes]
rs8033291	0.84[EUR][1000 genomes]
rs8034428	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8038466	0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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	esv1845471	chr15:54556063-54685463	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr15:54547000-54652600	Weak transcription	Fetal Lung	lung
2	chr15:54570800-54571600	Enhancers	Skeletal Muscle Female	skeletal muscle
3	chr15:54571200-54571800	Enhancers	Aorta	Aorta
4	chr15:54571400-54571800	Enhancers	Adipose Nuclei	Adipose

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