Variant report

Variant	rs7081239
Chromosome Location	chr10:56478392-56478393
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10825379	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10825380	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10825381	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10825390	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs11004454	1.00[ASN][1000 genomes]
rs11004456	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11004457	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11004458	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11004459	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11004461	1.00[ASN][1000 genomes]
rs11004462	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11004463	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs11004464	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs11004465	1.00[CHB][hapmap]
rs11004466	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs11004470	1.00[CEU][hapmap];0.85[CHB][hapmap]
rs11004473	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs11004474	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs11004480	1.00[CEU][hapmap];0.86[CHB][hapmap];0.90[YRI][hapmap]
rs11004487	1.00[CEU][hapmap]
rs11004490	1.00[CHB][hapmap]
rs11004491	0.85[CHB][hapmap]
rs11004495	1.00[CEU][hapmap]
rs11004515	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs11004526	1.00[CHB][hapmap]
rs11004528	1.00[CHB][hapmap]
rs11004529	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs11004530	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[YRI][hapmap]
rs11004531	1.00[CHB][hapmap]
rs11004532	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs11004535	1.00[CHB][hapmap]
rs11004556	1.00[CHB][hapmap]
rs11004574	1.00[CHB][hapmap]
rs12217615	1.00[CHB][hapmap]
rs12220692	1.00[CHB][hapmap]
rs12220919	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs12220935	1.00[CHB][hapmap]
rs1414690	1.00[CHB][hapmap];0.95[YRI][hapmap]
rs16906482	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs17592217	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1832185	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs1932601	1.00[CEU][hapmap];0.85[YRI][hapmap];0.97[EUR][1000 genomes]
rs1932602	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs2384520	1.00[CHB][hapmap]
rs2384526	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs4935118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4935119	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4935120	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4935536	0.87[CEU][hapmap]
rs4935540	1.00[CHB][hapmap]
rs4935543	1.00[CHB][hapmap]
rs4935545	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4935554	1.00[CHB][hapmap]
rs4935555	1.00[CEU][hapmap];0.95[YRI][hapmap]
rs4935556	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs4935557	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs58286973	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67776107	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7073425	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7086634	1.00[CHB][hapmap]
rs7086650	1.00[CHB][hapmap]
rs7087693	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs72794533	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72794592	0.81[EUR][1000 genomes]
rs7900549	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7905280	0.85[CHB][hapmap]
rs953128	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:22 , 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	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
4	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
5	nsv550970	chr10:56361499-56764751	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
6	esv2758221	chr10:56408027-56566137	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv2759754	chr10:56408027-56566137	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv895447	chr10:56428277-56587755	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv1829325	chr10:56442061-56514009	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv550975	chr10:56448886-56494301	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1043472	chr10:56452937-56479771	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv895448	chr10:56456576-56526747	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv1039277	chr10:56456775-56485231	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv1838177	chr10:56462471-56478751	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv1831037	chr10:56462471-56494301	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv526545	chr10:56462471-56554972	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv1825751	chr10:56467657-56494207	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv1832833	chr10:56467874-56494301	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv1826456	chr10:56468563-56493670	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv14427	chr10:56469623-56503557	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv1830646	chr10:56473373-56493670	Inactive region	Chromatin interactive region	n/a	n/a	diseases
22	nsv1053651	chr10:56478151-56545395	Enhancers Weak transcription	Chromatin interactive region	n/a	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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