Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:84282789..84284705-chr14:84293258..84295576,2	MCF-7	breast:
2	chr14:84292171..84294967-chr14:84304477..84306889,2	MCF-7	breast:

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

rs_ID	r²[population]
rs10137336	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10146014	0.91[ASN][1000 genomes]
rs10149682	0.91[ASN][1000 genomes]
rs10149704	0.89[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs10150517	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12586637	0.89[ASN][1000 genomes]
rs12588002	0.93[ASN][1000 genomes]
rs1511318	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1698258	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1705662	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17119147	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17119189	0.87[ASN][1000 genomes]
rs17637116	0.87[ASN][1000 genomes]
rs17643817	0.91[ASN][1000 genomes]
rs17710375	0.90[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs17711443	0.91[ASN][1000 genomes]
rs17711598	0.91[ASN][1000 genomes]
rs28693875	0.96[ASN][1000 genomes]
rs55959064	0.87[ASN][1000 genomes]
rs57002888	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59712100	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7145520	0.90[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs7156850	0.89[ASN][1000 genomes]
rs72697171	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72697173	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72697185	0.89[ASN][1000 genomes]
rs8003919	0.87[ASN][1000 genomes]
rs9323741	0.96[ASN][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	esv2751287	chr14:84294487-84338247	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84292800-84294600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr14:84293200-84295000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr14:84293400-84295400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr14:84293800-84294800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr14:84294200-84295000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr14:84294400-84295200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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