Variant report

Variant	rs7843946
Chromosome Location	chr8:39130784-39130785
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:39130457..39132494-chr8:39133684..39136395,2	K562	blood:
2	chr8:38964583..38965453-chr8:39130431..39131111,2	MCF-7	breast:
3	chr8:38964712..38965432-chr8:39130166..39131088,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000197140	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10088174	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10093393	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10808920	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10958543	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11776234	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11777253	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11782591	0.81[EUR][1000 genomes]
rs11786406	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12675132	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12679074	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12682638	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28460316	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28649569	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28788037	0.81[EUR][1000 genomes]
rs28795368	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4128223	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4316117	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4515515	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4585713	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4733912	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4733992	0.81[EUR][1000 genomes]
rs4733994	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55759907	0.80[EUR][1000 genomes]
rs55817221	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56093547	0.80[EUR][1000 genomes]
rs57822948	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58036010	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6474126	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6988280	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6989252	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7001103	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7013701	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7016661	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72500200	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73606793	0.81[EUR][1000 genomes]
rs73608630	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73608634	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73608636	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7464434	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7816763	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7843723	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015907	chr8:38967169-39718559	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv539550	chr8:38967169-39718559	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1027443	chr8:38993423-39181079	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv539551	chr8:38993423-39181079	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv428198	chr8:39069309-39405724	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1019752	chr8:39087542-39371410	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv1798122	chr8:39101565-39405724	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv1809741	chr8:39101565-39405724	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	esv1815710	chr8:39101565-39405724	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	esv1827982	chr8:39101565-39405724	ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	esv1829387	chr8:39101565-39405724	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	esv1845167	chr8:39101565-39405724	Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	esv3421887	chr8:39103844-39132832	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	esv1845068	chr8:39120649-39452805	Bivalent Enhancer Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	esv3326433	chr8:39128770-39131746	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39129200-39131200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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