Variant report

Variant	rs7772343
Chromosome Location	chr6:102355883-102355884
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1340276	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs1340277	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs1340288	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1475919	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.96[ASN][1000 genomes]
rs1475920	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1475921	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1475922	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1475923	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1475924	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1475925	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1578291	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1578294	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1967944	0.96[ASN][1000 genomes]
rs2051446	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2051449	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2246086	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2518186	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2518187	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2518188	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2518189	0.96[ASN][1000 genomes]
rs2518211	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2518214	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2518274	0.93[ASN][1000 genomes]
rs2518276	0.90[ASN][1000 genomes]
rs2791762	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2791763	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2791765	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2791766	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2791767	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2791774	0.89[ASN][1000 genomes]
rs2791790	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2791791	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2791801	0.82[CHB][hapmap]
rs5021084	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9404156	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs9498740	0.82[JPT][hapmap]

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	nsv1032499	chr6:102069885-102720998	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv830743	chr6:102284082-102459192	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv886465	chr6:102318339-102466397	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv886466	chr6:102327303-102432398	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv470850	chr6:102343078-102595587	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:102355200-102356000	Enhancers	HepG2	liver
2	chr6:102355600-102356000	Flanking Active TSS	Liver	Liver

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