Variant report

Variant	rs8113780
Chromosome Location	chr19:42344819-42344820
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:42344282..42346616-chr19:42346629..42348983,3	MCF-7	breast:
2	chr19:42339358..42341430-chr19:42344625..42347180,2	MCF-7	breast:
3	chr19:42337138..42340110-chr19:42342013..42344959,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000142025	Chromatin interaction
ENSG00000183103	Chromatin interaction
ENSG00000267839	Chromatin interaction

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10401370	0.81[ASN][1000 genomes]
rs10401528	0.83[ASN][1000 genomes]
rs10401928	0.86[ASN][1000 genomes]
rs10404939	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10407206	0.89[ASN][1000 genomes]
rs10407619	0.86[ASN][1000 genomes]
rs10407797	0.86[ASN][1000 genomes]
rs10408367	0.82[ASN][1000 genomes]
rs10410918	0.87[ASN][1000 genomes]
rs10414356	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10414823	0.93[ASN][1000 genomes]
rs10416824	0.84[ASN][1000 genomes]
rs10426243	0.81[ASN][1000 genomes]
rs10500284	0.97[ASN][1000 genomes]
rs12461099	0.82[ASN][1000 genomes]
rs12461131	0.82[ASN][1000 genomes]
rs12971550	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12976571	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12979253	0.92[ASN][1000 genomes]
rs12984383	0.82[ASN][1000 genomes]
rs1366610	0.82[ASN][1000 genomes]
rs1457144	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1811564	0.82[ASN][1000 genomes]
rs1870093	0.81[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2008798	0.86[ASN][1000 genomes]
rs2008808	0.83[ASN][1000 genomes]
rs2075749	0.82[ASN][1000 genomes]
rs2075750	0.81[ASN][1000 genomes]
rs2075752	0.81[ASN][1000 genomes]
rs2199829	0.85[ASN][1000 genomes]
rs2199830	0.87[ASN][1000 genomes]
rs2290695	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2305809	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28821622	0.88[ASN][1000 genomes]
rs28824227	0.93[ASN][1000 genomes]
rs3786536	0.81[ASN][1000 genomes]
rs3786538	0.82[ASN][1000 genomes]
rs3795022	0.85[ASN][1000 genomes]
rs3922888	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4130852	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4480913	0.85[ASN][1000 genomes]
rs4803511	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4803512	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58857981	0.82[ASN][1000 genomes]
rs6508998	0.87[ASN][1000 genomes]
rs6508999	0.93[ASN][1000 genomes]
rs6509000	0.93[ASN][1000 genomes]
rs6509001	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6509002	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7248641	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7250787	0.82[ASN][1000 genomes]
rs7252877	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7254214	0.82[ASN][1000 genomes]
rs7257666	0.83[ASN][1000 genomes]
rs7259596	0.82[ASN][1000 genomes]
rs734107	0.85[ASN][1000 genomes]
rs73549152	0.82[ASN][1000 genomes]
rs8099934	0.87[ASN][1000 genomes]
rs8100182	0.86[ASN][1000 genomes]
rs8104958	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8106505	0.93[ASN][1000 genomes]
rs8110199	0.87[ASN][1000 genomes]
rs8113283	0.82[ASN][1000 genomes]
rs8113538	0.82[ASN][1000 genomes]
rs8113641	0.82[ASN][1000 genomes]
rs8113720	0.82[ASN][1000 genomes]
rs8113741	0.82[ASN][1000 genomes]
rs8113813	0.82[ASN][1000 genomes]
rs873282	0.82[ASN][1000 genomes]
rs899662	0.86[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	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv1061878	chr19:42325490-42416056	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv911776	chr19:42343526-42416056	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42344000-42345000	Enhancers	Primary monocytes fromperipheralblood	blood

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