Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:59636747..59637753-chr5:59650701..59651624,3	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10939840	0.95[TSI][hapmap]
rs10939842	0.90[TSI][hapmap]
rs12153271	0.89[TSI][hapmap]
rs16877896	1.00[JPT][hapmap]
rs16877898	1.00[JPT][hapmap]
rs16877901	1.00[JPT][hapmap]
rs16877912	0.90[TSI][hapmap]
rs4547892	0.94[ASW][hapmap];1.00[CEU][hapmap];0.87[GIH][hapmap];0.93[LWK][hapmap];0.94[MKK][hapmap];0.87[TSI][hapmap];0.82[YRI][hapmap];0.87[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs56247947	0.97[ASN][1000 genomes]
rs57177718	0.96[ASN][1000 genomes]
rs58512371	0.99[ASN][1000 genomes]
rs59014679	0.99[ASN][1000 genomes]
rs59576667	0.99[ASN][1000 genomes]
rs59578756	0.99[ASN][1000 genomes]
rs6865707	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs73106775	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73106780	0.86[ASN][1000 genomes]
rs73106781	0.99[ASN][1000 genomes]
rs73106782	1.00[ASN][1000 genomes]
rs7707365	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025856	chr5:59188419-59928852	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv830316	chr5:59480269-59689829	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv598288	chr5:59627555-60003460	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59625200-59646800	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59635200-59638600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr5:59635800-59637600	Enhancers	GM12878-XiMat	blood
4	chr5:59635800-59639200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr5:59636000-59637800	Enhancers	Fetal Brain Male	brain
6	chr5:59636600-59637800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:59637000-59637600	Enhancers	Stomach Smooth Muscle	stomach
8	chr5:59637200-59637800	Enhancers	Aorta	Aorta
9	chr5:59637400-59637800	Weak transcription	Fetal Brain Female	brain
10	chr5:59637400-59639200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr5:59637400-59642000	Weak transcription	Muscle Satellite Cultured Cells	--

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