Variant report

Variant	rs7631658
Chromosome Location	chr3:46268970-46268971
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	chr3:46268227..46270497-chr3:46275042..46277907,2	MCF-7	breast:
2	chr3:46262763..46265229-chr3:46268734..46270936,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11914967	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11918542	0.85[AMR][1000 genomes]
rs11919943	0.82[YRI][hapmap]
rs11926063	0.96[YRI][hapmap];0.87[AFR][1000 genomes]
rs11929424	0.85[AMR][1000 genomes]
rs11929453	0.85[AMR][1000 genomes]
rs11929460	0.85[AMR][1000 genomes]
rs11929489	0.83[AFR][1000 genomes]
rs13062523	0.83[AFR][1000 genomes]
rs13088766	0.93[YRI][hapmap];0.83[AFR][1000 genomes]
rs17078685	0.85[AMR][1000 genomes]
rs17078689	0.85[AMR][1000 genomes]
rs2373156	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs3136663	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34498313	0.83[AFR][1000 genomes]
rs34985947	0.81[AFR][1000 genomes]
rs35195804	0.83[AFR][1000 genomes]
rs35481399	0.91[AFR][1000 genomes]
rs35678191	0.87[AFR][1000 genomes]
rs35984988	0.83[AFR][1000 genomes]
rs41537946	0.83[AFR][1000 genomes]
rs56093858	0.85[AMR][1000 genomes]
rs56277808	0.85[AMR][1000 genomes]
rs56698532	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57115330	0.82[AFR][1000 genomes]
rs57560436	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59340338	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60714453	0.85[AMR][1000 genomes]
rs71327043	0.92[AFR][1000 genomes]
rs71327044	0.87[AFR][1000 genomes]
rs73830780	0.85[AMR][1000 genomes]
rs73830781	0.85[AMR][1000 genomes]
rs73830796	0.85[AMR][1000 genomes]
rs73833005	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73833018	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73833020	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7615337	0.85[AMR][1000 genomes]
rs7618935	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7620586	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs7628489	0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs7651539	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs7653045	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876734	chr3:45725031-46468467	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv498008	chr3:45733423-46319401	Strong transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 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	chr3:46263600-46270000	Weak transcription	Fetal Lung	lung
2	chr3:46264200-46269600	Weak transcription	Placenta	Placenta
3	chr3:46264400-46276400	Weak transcription	Fetal Thymus	thymus
4	chr3:46265600-46270000	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr3:46265600-46276400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr3:46265800-46269400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr3:46267400-46269200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:46267600-46269000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr3:46268000-46269400	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr3:46268600-46270800	Enhancers	Primary B cells from cord blood	blood

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