Variant report

Variant	rs9470271
Chromosome Location	chr6:11860757-11860758
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:11854081..11855921-chr6:11860130..11862778,2	MCF-7	breast:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10947602	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10947610	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11755122	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1883854	0.97[ASN][1000 genomes]
rs1883855	0.97[ASN][1000 genomes]
rs1883857	0.91[ASN][1000 genomes]
rs2002735	0.85[ASN][1000 genomes]
rs2002736	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2015055	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4520010	0.96[ASN][1000 genomes]
rs4521583	0.98[ASN][1000 genomes]
rs4526189	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4711437	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4713966	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6457919	0.93[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6916995	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6921169	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7450581	0.98[ASN][1000 genomes]
rs7745004	0.95[CEU][hapmap];0.88[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7765341	0.96[ASN][1000 genomes]
rs7767287	0.97[ASN][1000 genomes]
rs7769049	0.95[ASN][1000 genomes]
rs932441	0.97[ASN][1000 genomes]
rs9357210	0.97[ASN][1000 genomes]
rs9394332	0.87[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs9462160	0.87[CHB][hapmap];0.88[JPT][hapmap];0.84[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	nsv5201	chr6:11833966-11879236	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11852000-11866200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:11858600-11863000	Strong transcription	Liver	Liver
3	chr6:11859800-11867000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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