Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:116046151..116048173-chr3:116049093..116051195,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11918762	1.00[CHB][hapmap];0.83[CHD][hapmap]
rs13073491	1.00[CHB][hapmap]
rs13320911	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs13321959	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes]
rs16824799	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1712999	0.83[CHD][hapmap];1.00[JPT][hapmap]
rs17646052	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17652825	0.96[EUR][1000 genomes]
rs17702596	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17704285	1.00[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs1835672	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4831093	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6438312	1.00[CHB][hapmap];0.83[CHD][hapmap]
rs6775293	1.00[CHB][hapmap]
rs6809953	1.00[CHB][hapmap];0.83[CHD][hapmap]
rs72950135	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7611085	1.00[CHD][hapmap]
rs957783	1.00[CHB][hapmap];0.83[CHD][hapmap]
rs9822049	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9836288	0.96[EUR][1000 genomes]
rs9869252	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes]
rs9877364	1.00[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877361	chr3:116017931-116138039	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr3:116046200-116058000	Weak transcription	Colon Smooth Muscle	Colon
2	chr3:116049600-116052000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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