Variant report

Variant	rs1219784
Chromosome Location	chr10:56326035-56326036
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10128484	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[TSI][hapmap]
rs10509015	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs10740585	0.94[EUR][1000 genomes]
rs10763116	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs10825359	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs10825360	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs10825361	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs1219783	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs1219785	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap]
rs1930150	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs1930151	1.00[CHB][hapmap]
rs1930152	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs1930153	1.00[CEU][hapmap]
rs1930155	0.94[EUR][1000 genomes]
rs1930156	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes]
rs1930157	0.94[EUR][1000 genomes]
rs1930175	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];0.90[TSI][hapmap]
rs1937405	1.00[CHB][hapmap]
rs1937407	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes]
rs1937410	1.00[CEU][hapmap];0.90[TSI][hapmap]
rs1937413	1.00[CEU][hapmap]
rs1937414	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[TSI][hapmap]
rs1937417	1.00[CEU][hapmap]
rs1937419	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[TSI][hapmap]
rs1937420	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs2026409	1.00[CEU][hapmap]
rs2026411	1.00[CEU][hapmap]
rs2026413	1.00[CEU][hapmap]
rs2104890	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs2154267	1.00[CEU][hapmap];0.90[TSI][hapmap]
rs2384473	1.00[CEU][hapmap]
rs2489897	1.00[CHB][hapmap]
rs4381287	0.94[EUR][1000 genomes]
rs4503435	1.00[CEU][hapmap]
rs4520501	0.94[EUR][1000 genomes]
rs4935523	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[TSI][hapmap]
rs6481106	1.00[CEU][hapmap];0.90[TSI][hapmap]
rs6481107	1.00[CEU][hapmap];0.90[TSI][hapmap]
rs7076026	0.94[EUR][1000 genomes]
rs7089865	1.00[CEU][hapmap]
rs7096402	0.89[EUR][1000 genomes]
rs7099058	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[TSI][hapmap]
rs7903258	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs7903542	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs7919479	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs7919697	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs7922800	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs949689	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes]
rs949690	0.94[EUR][1000 genomes]
rs951434	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs9633607	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs9633609	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs9971344	1.00[CEU][hapmap];1.00[CHB][hapmap]

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	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	nsv550968	chr10:56319852-56343345	Enhancers	lncRNA	n/a	inside rSNPs	diseases
7	nsv467228	chr10:56322477-56343345	Enhancers	lncRNA	n/a	inside rSNPs	diseases
8	nsv550969	chr10:56322477-56343345	Enhancers	lncRNA	n/a	inside rSNPs	diseases

No data

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

No data

Quick Search:

Input of quick search could be:

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

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links