Variant report

Variant	rs6016809
Chromosome Location	chr20:41122834-41122835
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10485694	1.00[ASN][1000 genomes]
rs11904854	1.00[ASN][1000 genomes]
rs11906033	1.00[ASN][1000 genomes]
rs11907808	1.00[ASN][1000 genomes]
rs2049969	1.00[ASN][1000 genomes]
rs35041089	1.00[ASN][1000 genomes]
rs35324452	1.00[ASN][1000 genomes]
rs35762999	1.00[ASN][1000 genomes]
rs35800638	1.00[ASN][1000 genomes]
rs57772475	1.00[ASN][1000 genomes]
rs57920496	1.00[ASN][1000 genomes]
rs6016806	1.00[ASN][1000 genomes]
rs6016807	1.00[MEX][hapmap];1.00[ASN][1000 genomes]
rs6016808	1.00[ASN][1000 genomes]
rs6016810	1.00[MEX][hapmap];1.00[ASN][1000 genomes]
rs6016811	1.00[MEX][hapmap]
rs6016813	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6030273	1.00[ASN][1000 genomes]
rs6030274	1.00[MEX][hapmap];1.00[ASN][1000 genomes]
rs6030275	1.00[ASN][1000 genomes]
rs6030276	1.00[ASN][1000 genomes]
rs6030277	1.00[MEX][hapmap];1.00[ASN][1000 genomes]
rs6030282	1.00[ASN][1000 genomes]
rs6030286	1.00[ASN][1000 genomes]
rs6030289	1.00[ASN][1000 genomes]
rs6093659	1.00[MEX][hapmap];1.00[ASN][1000 genomes]
rs6093660	1.00[MEX][hapmap];1.00[ASN][1000 genomes]
rs6093684	1.00[MEX][hapmap]
rs6093704	1.00[MEX][hapmap]
rs6102825	1.00[ASN][1000 genomes]
rs6102855	1.00[ASN][1000 genomes]
rs6102856	1.00[ASN][1000 genomes]
rs6102859	1.00[ASN][1000 genomes]
rs6102860	1.00[MEX][hapmap];1.00[ASN][1000 genomes]
rs6102863	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6102870	1.00[ASN][1000 genomes]
rs6102871	1.00[ASN][1000 genomes]
rs6102943	1.00[MEX][hapmap]
rs6102945	1.00[MEX][hapmap]
rs6102947	1.00[MEX][hapmap]
rs6102959	1.00[MEX][hapmap]
rs7263792	1.00[ASN][1000 genomes]
rs73271582	1.00[ASN][1000 genomes]
rs73271583	1.00[ASN][1000 genomes]
rs73273400	1.00[ASN][1000 genomes]
rs73908945	1.00[ASN][1000 genomes]
rs8118149	1.00[ASN][1000 genomes]
rs8122692	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	esv1807209	chr20:41107678-41154898	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41113600-41125600	Weak transcription	Pancreas	Pancrea
2	chr20:41122800-41123000	Enhancers	HUES64 Cell Line	embryonic stem cell

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