Variant report

Variant	rs7846084
Chromosome Location	chr8:51595477-51595478
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	chr8:51590048..51591794-chr8:51592149..51596284,3	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10086876	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10099354	0.97[ASN][1000 genomes]
rs10099939	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10481271	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12676534	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12678401	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16915275	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs16915315	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs16915358	0.92[ASN][1000 genomes]
rs1911832	0.92[ASN][1000 genomes]
rs28520704	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28830520	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28875312	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs41364346	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4146358	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4146359	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs56267139	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58540522	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59347506	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6473289	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6473290	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6473320	0.92[ASN][1000 genomes]
rs6985954	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6987141	0.97[ASN][1000 genomes]
rs6988284	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6989519	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6992531	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6998678	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7009493	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7012490	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7016907	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7017534	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7017695	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7017813	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73569441	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73571208	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7820529	0.92[ASN][1000 genomes]
rs7821535	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7824055	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7824609	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7841003	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9298378	0.92[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	nsv948436	chr8:51115028-51917504	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv429914	chr8:51371447-51617647	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv531502	chr8:51390997-51703556	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3514165	chr8:51416583-51923545	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv3514166	chr8:51416583-51923545	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv890873	chr8:51462163-51612641	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv1027452	chr8:51525439-51725489	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51592000-51596000	Weak transcription	Brain Germinal Matrix	brain
2	chr8:51594400-51596200	Enhancers	Liver	Liver
3	chr8:51594600-51596400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:51595200-51595600	Enhancers	Fetal Intestine Large	intestine
5	chr8:51595200-51595800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:51595200-51596400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr8:51595200-51596600	Enhancers	NH-A	brain
8	chr8:51595200-51596800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr8:51595400-51596400	Enhancers	HUVEC	blood vessel

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