Variant report

Variant	rs2059593
Chromosome Location	chr15:39087905-39087906
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	chr15:39085713..39088566-chr15:39372910..39375619,2	MCF-7	breast:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1004451	0.89[EUR][1000 genomes]
rs1004864	0.89[EUR][1000 genomes]
rs10459670	0.92[CEU][hapmap];0.87[TSI][hapmap]
rs10520107	0.90[EUR][1000 genomes]
rs10520111	0.89[EUR][1000 genomes]
rs11630569	0.92[EUR][1000 genomes]
rs11631203	0.87[EUR][1000 genomes]
rs11632268	0.87[EUR][1000 genomes]
rs11635756	0.87[EUR][1000 genomes]
rs11636712	0.82[EUR][1000 genomes]
rs12372928	0.83[EUR][1000 genomes]
rs12902075	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12902084	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12915426	0.90[EUR][1000 genomes]
rs12916389	0.84[EUR][1000 genomes]
rs17117	0.92[EUR][1000 genomes]
rs2912393	0.97[ASN][1000 genomes]
rs2958278	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2958306	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4429264	0.89[EUR][1000 genomes]
rs4602012	0.89[EUR][1000 genomes]
rs4924300	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8029046	0.82[EUR][1000 genomes]
rs8040011	0.89[EUR][1000 genomes]
rs8040794	0.84[EUR][1000 genomes]
rs8040905	0.82[EUR][1000 genomes]
rs8041441	0.83[EUR][1000 genomes]
rs8042816	0.89[EUR][1000 genomes]

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	nsv1046994	chr15:38806163-39239014	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv832975	chr15:39011915-39227590	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1054810	chr15:39019900-39578526	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv542359	chr15:39019900-39578526	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv471239	chr15:39048231-39097273	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv457116	chr15:39048231-39098349	Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv569206	chr15:39048231-39098349	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv904087	chr15:39065424-39117186	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv510659	chr15:39072035-39148591	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv904088	chr15:39081717-39117186	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 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	chr15:39087600-39088000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr15:39087600-39088000	Enhancers	Fetal Lung	lung
3	chr15:39087600-39088800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr15:39087800-39088000	Enhancers	HSMMtube	muscle

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