Variant report

Variant	rs6513812
Chromosome Location	chr20:41382183-41382184
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1015314	0.93[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12479759	1.00[CHB][hapmap]
rs1885832	1.00[CHB][hapmap]
rs1885833	1.00[CHB][hapmap]
rs2206905	1.00[CHB][hapmap]
rs3746533	0.93[CEU][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6016859	1.00[CHB][hapmap]
rs6065531	0.93[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6065532	0.93[CEU][hapmap];0.92[EUR][1000 genomes]
rs6065533	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6065534	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6072856	0.93[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6072857	0.92[CEU][hapmap];0.93[EUR][1000 genomes]
rs6072858	0.93[CEU][hapmap];0.91[EUR][1000 genomes]
rs6072859	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6072860	0.93[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6072861	0.93[CEU][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6072862	0.93[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6072864	0.93[CEU][hapmap];0.85[EUR][1000 genomes]
rs6072865	0.93[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6072866	1.00[ASN][1000 genomes]
rs6072868	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7261386	1.00[CHB][hapmap]
rs73907265	1.00[ASN][1000 genomes]
rs9808582	0.93[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915994	chr20:41180550-41464507	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1058990	chr20:41289969-41543912	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv544277	chr20:41289969-41543912	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41378800-41385800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr20:41379400-41383600	Weak transcription	Lung	lung
3	chr20:41380400-41384400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr20:41381800-41383800	Weak transcription	Stomach Mucosa	stomach
5	chr20:41382000-41383600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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