Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:102349024..102351373-chr11:102352689..102355274,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11225264	1.00[ASW][hapmap];1.00[MKK][hapmap]
rs11225266	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11225278	1.00[AFR][1000 genomes]
rs11225285	1.00[ASW][hapmap]
rs11225286	1.00[AFR][1000 genomes]
rs11225287	1.00[AFR][1000 genomes]
rs11225290	1.00[AFR][1000 genomes]
rs11225297	1.00[AFR][1000 genomes]
rs11225299	1.00[AFR][1000 genomes]
rs11225300	1.00[AFR][1000 genomes]
rs11547915	1.00[ASW][hapmap];1.00[AFR][1000 genomes]
rs11605066	1.00[AFR][1000 genomes]
rs11605133	1.00[ASW][hapmap]
rs11605915	1.00[AFR][1000 genomes]
rs11607657	1.00[AFR][1000 genomes]
rs11607908	1.00[AFR][1000 genomes]
rs12184413	1.00[AFR][1000 genomes]
rs1318199	1.00[AFR][1000 genomes]
rs17098230	1.00[AFR][1000 genomes]
rs17350205	1.00[AFR][1000 genomes]
rs17769668	1.00[AFR][1000 genomes]
rs2078237	0.93[ASN][1000 genomes]
rs34296997	1.00[AFR][1000 genomes]
rs35457182	1.00[AFR][1000 genomes]
rs35569122	1.00[AFR][1000 genomes]
rs35972941	1.00[AFR][1000 genomes]
rs57346058	1.00[AFR][1000 genomes]
rs57562739	1.00[AFR][1000 genomes]
rs58250524	1.00[AFR][1000 genomes]
rs60056981	1.00[AFR][1000 genomes]
rs61334418	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035567	chr11:102264516-102431607	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv469990	chr11:102335609-102413943	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv556150	chr11:102335609-102415859	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv468854	chr11:102336617-102413943	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv556151	chr11:102336617-102413943	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr11:102341000-102359600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:102353400-102354200	Enhancers	Hela-S3	cervix
3	chr11:102353400-102361400	Enhancers	HepG2	liver
4	chr11:102353600-102356000	Weak transcription	Stomach Mucosa	stomach

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