Variant report

Variant	rs2207886
Chromosome Location	chr20:41166223-41166224
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1033642	0.87[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs1033643	0.88[CHB][hapmap];0.87[JPT][hapmap];0.84[MEX][hapmap];0.83[ASN][1000 genomes]
rs1569908	0.94[CHB][hapmap];0.87[JPT][hapmap];0.93[ASN][1000 genomes]
rs2064676	0.84[ASN][1000 genomes]
rs2064677	0.88[CHB][hapmap];0.87[JPT][hapmap];0.91[MEX][hapmap];0.84[ASN][1000 genomes]
rs2064678	0.88[CHB][hapmap];0.87[JPT][hapmap];0.92[MEX][hapmap];0.85[ASN][1000 genomes]
rs2205939	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2207885	0.81[JPT][hapmap]
rs6016816	0.86[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap]
rs6030291	0.86[CEU][hapmap];0.91[GIH][hapmap];0.81[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap]
rs6065496	0.93[JPT][hapmap]
rs6072758	1.00[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];0.84[MEX][hapmap];0.81[ASN][1000 genomes]
rs6072759	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs6072767	1.00[MEX][hapmap]
rs6072770	0.94[TSI][hapmap];0.84[EUR][1000 genomes]
rs6072773	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.92[MEX][hapmap];0.96[ASN][1000 genomes]
rs6072776	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6093656	0.82[CHD][hapmap]
rs6093657	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.82[ASN][1000 genomes]
rs6093669	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6093670	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6093672	0.87[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6093673	0.94[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs6102880	0.87[TSI][hapmap]
rs6102888	0.86[CEU][hapmap];0.96[GIH][hapmap];0.81[JPT][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap]
rs6102894	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6102895	0.84[MEX][hapmap]
rs6102897	0.81[ASN][1000 genomes]
rs6102899	0.82[CHB][hapmap]
rs73127302	0.88[ASN][1000 genomes]
rs8115216	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751913	chr20:40422982-41269321	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv833987	chr20:41007663-41184914	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
3	nsv1059852	chr20:41087948-41217672	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv544276	chr20:41087948-41217672	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1055546	chr20:41102999-41260749	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1064253	chr20:41120425-41379706	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1061449	chr20:41126720-41212178	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv586006	chr20:41157707-41290936	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2207886	RASSF9	trans	parietal	SCAN
rs2207886	YWHAB	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41160800-41173000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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