Variant report

Variant	rs9384867
Chromosome Location	chr6:113763719-113763720
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:113763198..113764987-chr6:114177471..114180396,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000155130	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10484458	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12175106	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12526316	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12527509	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12528387	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1883170	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2049924	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2142638	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2142640	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2179114	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2179115	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2179116	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2179117	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2348298	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2348299	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2348300	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2348301	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4945951	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs5001721	0.83[ASN][1000 genomes]
rs58748285	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6903255	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6925126	0.83[ASN][1000 genomes]
rs6928402	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs724290	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs766330	0.83[ASN][1000 genomes]
rs7766686	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs909542	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9320451	0.92[CEU][hapmap];0.96[CHB][hapmap];0.91[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9320452	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9320453	0.83[JPT][hapmap]
rs9320460	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9372363	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9372364	0.92[ASN][1000 genomes]
rs9374402	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9374403	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9374405	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9384868	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9387146	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9387147	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9387149	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9398344	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9398345	0.82[ASN][1000 genomes]
rs9398346	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9398347	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9400626	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9400630	0.84[ASN][1000 genomes]
rs9488196	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9488198	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9488199	0.81[ASN][1000 genomes]
rs9488202	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916294	chr6:113518489-113904305	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1034256	chr6:113703567-113793790	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1021815	chr6:113703567-113799956	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1018357	chr6:113748468-113781070	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv518991	chr6:113760526-113799618	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:113755800-113767800	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr6:113763400-113769000	Weak transcription	Placenta	Placenta
3	chr6:113763600-113763800	Enhancers	A549	lung

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