Variant report

Variant	rs1332210
Chromosome Location	chr9:9442915-9442916
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10117271	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs10119835	0.87[JPT][hapmap]
rs10491614	0.89[CEU][hapmap];0.88[CHB][hapmap];0.91[JPT][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10759074	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs10759075	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs10759076	0.81[JPT][hapmap]
rs10759078	0.85[CHB][hapmap]
rs10816128	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs10816129	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs10816133	0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs10816135	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs10816138	0.85[CHB][hapmap]
rs10816139	0.85[CHB][hapmap]
rs10816141	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs10816142	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs10977764	0.80[CHB][hapmap];0.90[JPT][hapmap]
rs10977778	0.88[CHB][hapmap];0.91[JPT][hapmap]
rs10977783	1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs10977787	0.84[ASN][1000 genomes]
rs10977792	0.80[ASN][1000 genomes]
rs10977793	0.84[ASN][1000 genomes]
rs10977800	0.85[CHB][hapmap]
rs1120438	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs11531684	0.88[CHB][hapmap];0.91[JPT][hapmap]
rs12686617	0.87[CHB][hapmap];0.91[JPT][hapmap]
rs1332192	0.81[CHB][hapmap];0.87[JPT][hapmap]
rs1332194	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs1332195	0.91[JPT][hapmap]
rs1332196	0.93[CHB][hapmap];0.87[JPT][hapmap]
rs1332209	0.86[ASN][1000 genomes]
rs1332212	0.81[JPT][hapmap]
rs1332213	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1332807	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1333107	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs1333108	0.90[JPT][hapmap]
rs1333114	0.88[CHB][hapmap];0.91[JPT][hapmap]
rs1412871	0.88[CHB][hapmap];0.86[JPT][hapmap]
rs1412872	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs1467790	0.88[CHB][hapmap];0.91[JPT][hapmap]
rs1576798	0.89[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs1576799	0.87[CHB][hapmap]
rs16929560	0.88[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs17831559	1.00[CHB][hapmap];0.87[JPT][hapmap];0.82[ASN][1000 genomes]
rs2026984	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs2382013	0.87[CHB][hapmap]
rs2382014	0.87[CHB][hapmap];0.87[JPT][hapmap]
rs2382015	0.87[CHB][hapmap];0.87[JPT][hapmap]
rs4237177	0.82[JPT][hapmap]
rs4388502	0.87[CHB][hapmap];0.87[JPT][hapmap]
rs4451355	0.92[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs4484751	0.87[CHB][hapmap]
rs4742602	0.82[JPT][hapmap]
rs7027963	0.87[JPT][hapmap]
rs7044905	0.85[CHB][hapmap];0.82[JPT][hapmap]
rs7465855	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs7468723	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs955474	0.86[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs987353	0.96[CEU][hapmap];0.93[CHB][hapmap];0.95[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498066	chr9:8961722-9486652	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv892252	chr9:9164473-9476425	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1025791	chr9:9294304-9626331	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv892258	chr9:9304839-9455711	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv892260	chr9:9350608-9474970	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv1016302	chr9:9355676-9549587	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv539982	chr9:9355676-9549587	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv892262	chr9:9382331-9445270	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	2 gene(s)	inside rSNPs	diseases
9	nsv613308	chr9:9409606-9750139	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv1023820	chr9:9414754-9468456	Weak transcription Enhancers	TF binding region	2 gene(s)	inside rSNPs	diseases
11	nsv1033808	chr9:9431799-9777960	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv528425	chr9:9437674-9556992	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv892264	chr9:9440838-9796577	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 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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