Variant report

Variant	rs58595226
Chromosome Location	chr2:99731407-99731408
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:99728152..99730874-chr2:99731119..99733166,2	MCF-7	breast:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10496334	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10496335	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11123760	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11123767	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11123768	0.93[EUR][1000 genomes]
rs11526114	0.86[EUR][1000 genomes]
rs12233087	0.86[EUR][1000 genomes]
rs12620997	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1586434	0.86[EUR][1000 genomes]
rs17022180	0.85[ASN][1000 genomes]
rs17022249	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2277876	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28785294	1.00[EUR][1000 genomes]
rs28794804	0.85[ASN][1000 genomes]
rs34751553	0.82[ASN][1000 genomes]
rs35071324	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35458525	0.82[ASN][1000 genomes]
rs3762472	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3791211	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4850895	0.84[ASN][1000 genomes]
rs56691336	0.82[ASN][1000 genomes]
rs56926889	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57273701	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57743480	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58635701	0.93[EUR][1000 genomes]
rs58745514	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59252741	0.84[ASN][1000 genomes]
rs59506582	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60056452	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60516303	0.85[ASN][1000 genomes]
rs60653099	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6719145	0.86[EUR][1000 genomes]
rs6746969	0.86[EUR][1000 genomes]
rs6748497	0.86[EUR][1000 genomes]
rs6749198	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7568749	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9752510	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431424	chr2:99652682-100494682	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv1013507	chr2:99729047-99861692	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 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	chr2:99718000-99740200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:99718600-99739600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:99723800-99739600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr2:99729400-99741600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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