Variant report

Variant	rs7896854
Chromosome Location	chr10:90896272-90896273
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10509564	0.99[ASN][1000 genomes]
rs10509565	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10887906	0.84[ASN][1000 genomes]
rs10887913	0.99[ASN][1000 genomes]
rs11202956	0.94[ASN][1000 genomes]
rs11202968	0.97[ASN][1000 genomes]
rs11202971	0.97[ASN][1000 genomes]
rs11202973	0.94[ASN][1000 genomes]
rs11202974	0.97[ASN][1000 genomes]
rs11202978	0.94[ASN][1000 genomes]
rs11202984	0.99[ASN][1000 genomes]
rs11202986	0.99[ASN][1000 genomes]
rs11202987	0.99[ASN][1000 genomes]
rs11202990	0.92[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs11202991	0.99[ASN][1000 genomes]
rs11202992	0.99[ASN][1000 genomes]
rs11202995	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs11202996	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12359686	0.99[ASN][1000 genomes]
rs1344234	0.83[ASN][1000 genomes]
rs17378555	0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs17378702	0.94[ASN][1000 genomes]
rs17380509	0.99[ASN][1000 genomes]
rs17380676	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17463822	0.97[ASN][1000 genomes]
rs17464831	0.99[ASN][1000 genomes]
rs17464997	0.99[ASN][1000 genomes]
rs17465248	0.92[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs1937324	0.94[ASN][1000 genomes]
rs2154249	0.99[ASN][1000 genomes]
rs2154250	0.99[ASN][1000 genomes]
rs2256329	0.84[ASN][1000 genomes]
rs2494647	0.83[ASN][1000 genomes]
rs28461567	0.99[ASN][1000 genomes]
rs28533190	0.99[ASN][1000 genomes]
rs2863221	0.94[ASN][1000 genomes]
rs2902448	0.96[ASN][1000 genomes]
rs7094057	0.97[ASN][1000 genomes]
rs72810981	0.90[ASN][1000 genomes]
rs72810994	0.97[ASN][1000 genomes]
rs72812827	0.99[ASN][1000 genomes]
rs72812830	0.99[ASN][1000 genomes]
rs72812831	0.99[ASN][1000 genomes]
rs72812833	0.99[ASN][1000 genomes]
rs72812834	0.99[ASN][1000 genomes]
rs72812845	0.99[ASN][1000 genomes]
rs72812848	0.99[ASN][1000 genomes]
rs72812849	0.99[ASN][1000 genomes]
rs72812851	0.99[ASN][1000 genomes]
rs72812855	0.99[ASN][1000 genomes]
rs72812859	0.99[ASN][1000 genomes]
rs72812860	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72812862	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72812886	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72812889	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72812894	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv831944	chr10:90822654-90967018	Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	esv2758235	chr10:90835064-91017486	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2759775	chr10:90835064-91017486	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv895881	chr10:90842431-90940003	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1041964	chr10:90861380-91378356	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
8	nsv551844	chr10:90879304-90899444	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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