Variant report

Variant	rs6850337
Chromosome Location	chr4:88233557-88233558
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:88225793..88228433-chr4:88233021..88235909,2	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1037813	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11097148	1.00[CHB][hapmap]
rs11945520	1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13103234	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs13108043	1.00[ASN][1000 genomes]
rs13134084	1.00[ASN][1000 genomes]
rs17030453	1.00[ASN][1000 genomes]
rs17703261	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs35658582	1.00[ASN][1000 genomes]
rs4079	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4305486	1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4505787	0.86[EUR][1000 genomes]
rs57455613	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57954253	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58336541	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59054114	0.86[EUR][1000 genomes]
rs59395199	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59526367	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62306540	1.00[ASN][1000 genomes]
rs6531974	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6531985	1.00[CHB][hapmap]
rs6811010	1.00[CHB][hapmap]
rs6817242	1.00[CHB][hapmap]
rs6817981	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6822384	1.00[ASN][1000 genomes]
rs6829145	1.00[ASN][1000 genomes]
rs6833678	1.00[CHB][hapmap]
rs6834947	1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6840247	1.00[CHB][hapmap]
rs6846149	1.00[CHB][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6846352	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6849846	1.00[CHB][hapmap]
rs72875519	1.00[ASN][1000 genomes]
rs73839171	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7655477	0.94[YRI][hapmap]
rs7655805	0.94[YRI][hapmap]
rs7662471	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7664479	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7668285	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7676494	1.00[CHB][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7677036	1.00[CHB][hapmap]
rs7682516	1.00[CHB][hapmap]
rs7682892	1.00[CHB][hapmap]
rs7686034	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9684766	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997750	chr4:87933945-88264127	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1007020	chr4:88046263-88235018	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv537169	chr4:88046263-88235018	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv870296	chr4:88173534-88295927	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv879527	chr4:88194170-88250203	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
6	esv1802846	chr4:88211056-88246450	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1004518	chr4:88218473-88354403	Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:88225400-88237800	Strong transcription	Liver	Liver
2	chr4:88228000-88239600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:88228400-88237800	Weak transcription	Hela-S3	cervix
4	chr4:88229000-88235600	Weak transcription	Pancreas	Pancrea
5	chr4:88229000-88245000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr4:88229600-88235800	Weak transcription	Ovary	ovary
7	chr4:88230000-88240000	Weak transcription	Brain Angular Gyrus	brain
8	chr4:88230600-88239600	Weak transcription	Primary T cells from cord blood	blood
9	chr4:88231200-88235600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:88231400-88237400	Weak transcription	Left Ventricle	heart

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