Variant report

Variant	rs6049410
Chromosome Location	chr20:24094691-24094692
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:24087517..24089373-chr20:24093201..24095054,2	MCF-7	breast:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs57816463	1.00[EUR][1000 genomes]
rs58712671	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58987530	1.00[EUR][1000 genomes]
rs60160675	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036649	0.96[ASN][1000 genomes]
rs6036659	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036660	1.00[ASN][1000 genomes]
rs60448850	1.00[EUR][1000 genomes]
rs6049396	0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs6049397	0.88[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs6049398	0.96[ASN][1000 genomes]
rs6049401	0.88[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs6049402	0.96[ASN][1000 genomes]
rs6049404	0.96[ASN][1000 genomes]
rs6049405	0.87[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6049406	0.90[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6049407	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6049408	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6049409	0.87[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6049411	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6049420	1.00[ASN][1000 genomes]
rs6049421	1.00[ASN][1000 genomes]
rs6076187	0.87[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs6106785	0.94[ASN][1000 genomes]
rs6114490	0.98[ASN][1000 genomes]
rs6114491	1.00[EUR][1000 genomes]
rs7264988	1.00[EUR][1000 genomes]
rs7271486	1.00[EUR][1000 genomes]
rs73334853	1.00[EUR][1000 genomes]
rs8115661	0.88[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs8119437	1.00[EUR][1000 genomes]
rs9967925	1.00[EUR][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	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1056491	chr20:23955040-24105080	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24083400-24096200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr20:24094200-24095000	Enhancers	Stomach Smooth Muscle	stomach
3	chr20:24094200-24095600	Weak transcription	Fetal Stomach	stomach
4	chr20:24094400-24098400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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