Variant report

Variant	rs9478354
Chromosome Location	chr6:150334366-150334367
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	chr6:150328123..150330822-chr6:150332783..150334807,2	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10155731	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11155696	1.00[CEU][hapmap];0.81[CHB][hapmap];0.94[JPT][hapmap];0.80[YRI][hapmap];0.89[EUR][1000 genomes]
rs11155697	0.89[EUR][1000 genomes]
rs11752529	0.91[EUR][1000 genomes]
rs11752629	0.86[EUR][1000 genomes]
rs11754987	1.00[CEU][hapmap];0.81[CHB][hapmap];0.94[JPT][hapmap];0.80[YRI][hapmap];0.89[EUR][1000 genomes]
rs11757186	0.90[EUR][1000 genomes]
rs12204988	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13198863	1.00[CEU][hapmap];0.81[CHB][hapmap];0.94[JPT][hapmap];0.80[YRI][hapmap];0.89[EUR][1000 genomes]
rs13209192	0.96[CEU][hapmap];0.81[CHB][hapmap];0.94[JPT][hapmap]
rs1543547	0.85[EUR][1000 genomes]
rs1853664	0.85[EUR][1000 genomes]
rs34006533	0.89[EUR][1000 genomes]
rs3860823	0.96[CEU][hapmap];0.81[CHB][hapmap];0.94[JPT][hapmap];0.85[EUR][1000 genomes]
rs4086064	0.89[EUR][1000 genomes]
rs5006620	0.87[CHB][hapmap];0.85[JPT][hapmap];0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs5017312	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5017313	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5017314	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5017315	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs5017316	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs562425	0.81[CHB][hapmap];0.94[JPT][hapmap]
rs563278	0.96[CEU][hapmap];0.81[CHB][hapmap];0.94[JPT][hapmap];0.82[EUR][1000 genomes]
rs61730071	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72561813	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs763574	0.81[CHB][hapmap];0.94[JPT][hapmap];0.89[EUR][1000 genomes]
rs9478362	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9478380	0.89[EUR][1000 genomes]
rs9479403	1.00[CEU][hapmap];0.81[CHB][hapmap];0.94[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9479404	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9479405	1.00[CEU][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9479429	0.86[EUR][1000 genomes]
rs9479478	0.85[EUR][1000 genomes]
rs9479481	0.89[EUR][1000 genomes]
rs9479482	0.89[EUR][1000 genomes]
rs9479513	0.96[CEU][hapmap];0.81[CHB][hapmap];0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886764	chr6:150114745-150393683	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv517022	chr6:150145001-150426272	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv970176	chr6:150319173-150343329	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv7375	chr6:150324114-150388625	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	esv3344440	chr6:150324131-150388650	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	esv3323918	chr6:150327978-150392099	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150330200-150336200	Weak transcription	Lung	lung
2	chr6:150334200-150334800	Bivalent Enhancer	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links