Variant report

Variant	rs7280764
Chromosome Location	chr21:40518825-40518826
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	chr21:40509643..40512150-chr21:40518013..40520045,2	MCF-7	breast:

Extended variants
information (count: 49 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1046289	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11700978	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1888490	0.91[CEU][hapmap]
rs2234545	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2297255	0.91[CEU][hapmap];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2410103	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2836936	0.91[CEU][hapmap];0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2836937	0.91[CEU][hapmap];0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2836941	0.91[CEU][hapmap];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2836946	0.91[CEU][hapmap];0.85[ASN][1000 genomes]
rs2836947	0.91[CEU][hapmap];0.85[ASN][1000 genomes]
rs2836962	0.91[CEU][hapmap]
rs2836963	0.91[CEU][hapmap]
rs2836970	0.91[CEU][hapmap]
rs2836976	0.91[CEU][hapmap]
rs2836978	0.91[CEU][hapmap]
rs2836979	0.91[CEU][hapmap]
rs28552370	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28734946	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs376720	0.91[CEU][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs379291	0.91[CEU][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs383965	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs420888	0.91[CEU][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs433013	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs446090	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs449428	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4816613	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4817994	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4817995	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4817997	0.91[CEU][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4817998	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs6517516	0.91[CEU][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6517517	0.91[CEU][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7278048	0.89[CEU][hapmap]
rs7281540	0.91[CEU][hapmap];0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs8126528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8127987	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8129850	0.91[CEU][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8130798	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9305665	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9305669	0.91[CEU][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9305670	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9975909	0.81[ASN][1000 genomes]
rs9977787	0.85[ASN][1000 genomes]
rs9979691	0.91[CEU][hapmap]
rs9981595	0.91[CEU][hapmap];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9984518	0.80[AMR][1000 genomes];0.88[ASN][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	nsv1061831	chr21:40376316-40583555	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv544443	chr21:40376316-40583555	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7280764	BRWD1	Cis_1M	lymphoblastoid	RTeQTL
rs7280764	BRWD1	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40514200-40520200	Weak transcription	Psoas Muscle	Psoas

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