Variant report

Variant	rs2593136
Chromosome Location	chr10:55725207-55725208
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 131 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:123)

rs_ID	r²[population]
rs10740557	0.84[CEU][hapmap]
rs10740558	0.84[CEU][hapmap]
rs10740560	0.82[JPT][hapmap]
rs10763020	0.83[CEU][hapmap]
rs10763021	0.84[CEU][hapmap]
rs10763022	0.83[CEU][hapmap]
rs10763024	0.84[CEU][hapmap]
rs10763025	0.84[CEU][hapmap]
rs10763027	0.84[CEU][hapmap]
rs10763038	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[YRI][hapmap]
rs10825138	0.84[CEU][hapmap]
rs10825156	0.84[CEU][hapmap]
rs10825157	0.87[CEU][hapmap]
rs10825185	0.85[CEU][hapmap]
rs11003893	0.84[CEU][hapmap]
rs11003916	0.85[JPT][hapmap]
rs11003918	0.87[CEU][hapmap]
rs11003919	0.84[CEU][hapmap]
rs11003921	0.85[JPT][hapmap]
rs11003964	0.86[CHB][hapmap]
rs11003968	0.83[CHB][hapmap];0.80[ASN][1000 genomes]
rs11003969	0.84[CEU][hapmap]
rs11003977	0.85[CHB][hapmap]
rs12570313	0.97[ASN][1000 genomes]
rs12571668	0.98[ASN][1000 genomes]
rs12571882	0.86[ASN][1000 genomes]
rs12572470	0.84[CHB][hapmap];0.97[ASN][1000 genomes]
rs16937813	0.85[JPT][hapmap]
rs1900421	0.88[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1900422	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1900423	0.84[CEU][hapmap]
rs1900444	0.88[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs1900446	0.84[AFR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1900450	0.84[CEU][hapmap]
rs1900451	0.84[CEU][hapmap]
rs1900453	0.87[CEU][hapmap]
rs1900458	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.82[AFR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1900459	0.88[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1911420	0.91[CEU][hapmap]
rs1911427	1.00[CEU][hapmap]
rs1911429	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1911430	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2121525	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2135718	0.91[CEU][hapmap]
rs2135723	0.81[CEU][hapmap]
rs2166620	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2166621	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2166628	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2174716	0.81[CEU][hapmap]
rs2253198	0.86[CHB][hapmap]
rs2253647	0.86[CHB][hapmap]
rs2384327	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2384328	0.84[CEU][hapmap]
rs2384340	0.87[CEU][hapmap]
rs2384343	0.92[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2446608	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs2446609	1.00[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2446610	0.80[EUR][1000 genomes]
rs2456699	0.96[CEU][hapmap]
rs2456701	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2593103	0.87[CEU][hapmap]
rs2593105	0.87[CEU][hapmap]
rs2593106	0.84[CEU][hapmap]
rs2593107	0.86[CEU][hapmap];0.93[CHB][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2593120	0.87[CEU][hapmap]
rs2593122	0.87[CEU][hapmap]
rs2593123	0.84[CEU][hapmap]
rs2593129	0.87[CEU][hapmap]
rs2593131	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2593133	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap]
rs2593135	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2610823	0.84[CEU][hapmap]
rs2610837	0.82[CEU][hapmap]
rs2610884	0.80[ASN][1000 genomes]
rs2610893	0.95[CEU][hapmap]
rs2610899	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs2610902	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs2610906	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2610908	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap]
rs2610909	0.96[CEU][hapmap]
rs2610910	0.96[CEU][hapmap];0.81[EUR][1000 genomes]
rs2610912	0.84[CEU][hapmap]
rs2610919	0.84[CEU][hapmap]
rs2660172	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2660173	1.00[CEU][hapmap];0.88[YRI][hapmap]
rs2660178	0.83[CEU][hapmap]
rs2660183	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2660184	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2660186	0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2660188	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2660190	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2660192	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2660197	0.96[CEU][hapmap]
rs2921912	0.84[CEU][hapmap]
rs2921924	0.84[CEU][hapmap]
rs2921925	0.87[CEU][hapmap]
rs2921926	0.84[CEU][hapmap]
rs2926391	0.84[CEU][hapmap]
rs2926397	0.87[CEU][hapmap]
rs2926408	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2926410	0.81[CEU][hapmap]
rs4376818	0.83[CHB][hapmap]
rs4478893	0.85[JPT][hapmap]
rs4935485	0.81[CEU][hapmap]
rs5003374	0.88[CEU][hapmap]
rs6481043	0.83[CEU][hapmap]
rs6481045	0.88[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7069577	0.81[CEU][hapmap]
rs7095839	0.84[CEU][hapmap]
rs7097365	0.85[JPT][hapmap]
rs7358220	0.86[CHB][hapmap]
rs7476991	0.96[CEU][hapmap]
rs7893789	0.84[CEU][hapmap]
rs7896419	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7896432	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7896582	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7899816	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7904289	0.84[CEU][hapmap]
rs7910658	0.87[CEU][hapmap]
rs7911482	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7912992	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7915856	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7920872	0.81[CEU][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	esv1842975	chr10:55378668-55736655	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv949692	chr10:55502542-55893206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv895429	chr10:55564355-55736655	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv895430	chr10:55645953-55736655	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1052939	chr10:55654719-55769239	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv467213	chr10:55662089-55725234	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv550949	chr10:55662089-55725234	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv869303	chr10:55714219-55857931	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	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