Variant report

Variant	rs7089865
Chromosome Location	chr10:56348015-56348016
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10128484	1.00[CEU][hapmap]
rs10509015	1.00[CEU][hapmap]
rs10763116	1.00[CEU][hapmap]
rs10763118	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10763119	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10763120	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs10825359	1.00[CEU][hapmap]
rs10825360	1.00[CEU][hapmap]
rs10825361	1.00[CEU][hapmap]
rs1219783	1.00[CEU][hapmap]
rs1219784	1.00[CEU][hapmap]
rs1219785	1.00[CEU][hapmap]
rs1892344	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1930150	1.00[CEU][hapmap]
rs1930152	1.00[CEU][hapmap]
rs1930153	1.00[CEU][hapmap]
rs1930156	1.00[CEU][hapmap]
rs1930158	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs1930175	1.00[CEU][hapmap]
rs1937407	1.00[CEU][hapmap]
rs1937410	1.00[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.87[EUR][1000 genomes]
rs1937413	1.00[CEU][hapmap];0.81[CHB][hapmap];0.89[JPT][hapmap]
rs1937414	1.00[CEU][hapmap]
rs1937415	0.93[CHB][hapmap];0.90[JPT][hapmap]
rs1937417	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs1937419	1.00[CEU][hapmap]
rs1937420	1.00[CEU][hapmap]
rs2026409	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs2026410	0.93[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2026411	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2026412	0.93[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2026413	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs2104890	1.00[CEU][hapmap]
rs2154267	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2384473	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4007216	0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4503435	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs4935523	1.00[CEU][hapmap]
rs4935525	0.80[CHB][hapmap]
rs6481106	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs6481107	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7092655	0.87[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7095317	0.81[CHB][hapmap]
rs7099058	1.00[CEU][hapmap]
rs7903258	1.00[CEU][hapmap]
rs7903542	1.00[CEU][hapmap]
rs7919479	1.00[CEU][hapmap]
rs7919697	1.00[CEU][hapmap]
rs7922800	1.00[CEU][hapmap]
rs949689	1.00[CEU][hapmap]
rs951434	1.00[CEU][hapmap]
rs951435	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs9633607	1.00[CEU][hapmap]
rs9633609	1.00[CEU][hapmap]
rs984915	0.93[CHB][hapmap];0.88[JPT][hapmap];0.99[ASN][1000 genomes]
rs9971344	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050405	chr10:56224676-56800009	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv540635	chr10:56224676-56800009	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv895444	chr10:56254206-56354118	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv6709	chr10:56303925-56348716	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
5	nsv933410	chr10:56319433-56713977	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1043144	chr10:56332903-56680265	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 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	chr10:56346800-56348800	Enhancers	HUVEC	blood vessel

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