Variant report

Variant	rs4141129
Chromosome Location	chr5:57027317-57027318
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:57012903..57015556-chr5:57025615..57027382,2	MCF-7	breast:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10063185	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10077005	1.00[ASN][1000 genomes]
rs10461637	0.89[EUR][1000 genomes]
rs10805498	0.86[EUR][1000 genomes]
rs10940571	0.86[EUR][1000 genomes]
rs10940572	0.86[EUR][1000 genomes]
rs10940573	0.86[EUR][1000 genomes]
rs10940575	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10940576	0.90[EUR][1000 genomes]
rs11742452	0.87[EUR][1000 genomes]
rs11955303	0.86[EUR][1000 genomes]
rs12523268	0.90[EUR][1000 genomes]
rs12654403	0.86[EUR][1000 genomes]
rs13157214	0.86[EUR][1000 genomes]
rs13162397	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13166729	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13176491	0.86[EUR][1000 genomes]
rs13177213	0.85[EUR][1000 genomes]
rs13183265	0.86[EUR][1000 genomes]
rs13184846	0.86[EUR][1000 genomes]
rs13185021	0.86[EUR][1000 genomes]
rs13185580	0.91[ASN][1000 genomes]
rs13186318	0.88[EUR][1000 genomes]
rs1558367	0.89[EUR][1000 genomes]
rs1860575	0.86[EUR][1000 genomes]
rs2017201	0.91[ASN][1000 genomes]
rs2041401	0.86[EUR][1000 genomes]
rs2041402	0.86[EUR][1000 genomes]
rs2041403	0.86[EUR][1000 genomes]
rs2041677	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2041678	1.00[ASN][1000 genomes]
rs2191445	1.00[ASN][1000 genomes]
rs2191446	1.00[ASN][1000 genomes]
rs2191447	0.86[EUR][1000 genomes]
rs2191448	0.91[ASN][1000 genomes]
rs2215418	0.86[EUR][1000 genomes]
rs2408845	0.86[EUR][1000 genomes]
rs2408846	1.00[ASN][1000 genomes]
rs2408847	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2408848	0.88[EUR][1000 genomes]
rs2408849	1.00[ASN][1000 genomes]
rs2898028	1.00[ASN][1000 genomes]
rs4699910	0.91[ASN][1000 genomes]
rs4700212	0.86[EUR][1000 genomes]
rs4700213	0.86[EUR][1000 genomes]
rs4700214	0.91[ASN][1000 genomes]
rs4700215	0.85[EUR][1000 genomes]
rs4700216	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4700217	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6450431	1.00[ASN][1000 genomes]
rs6860385	0.86[EUR][1000 genomes]
rs6872973	0.87[EUR][1000 genomes]
rs6885246	0.87[EUR][1000 genomes]
rs7711714	0.86[EUR][1000 genomes]
rs7725863	0.86[EUR][1000 genomes]
rs7726116	0.86[EUR][1000 genomes]
rs7732108	0.91[ASN][1000 genomes]
rs7737409	0.91[ASN][1000 genomes]
rs9292141	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs978225	0.86[EUR][1000 genomes]
rs984529	0.86[EUR][1000 genomes]
rs986101	0.91[ASN][1000 genomes]
rs991727	0.91[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	nsv525330	chr5:56931673-57320343	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2756302	chr5:56978143-57180143	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830310	chr5:56989346-57176006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2763454	chr5:57006531-57161140	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57021800-57029200	Weak transcription	Aorta	Aorta
2	chr5:57021800-57030400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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