Variant report

Variant	rs11161682
Chromosome Location	chr2:76933902-76933903
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1010058	0.93[EUR][1000 genomes]
rs10873722	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10873723	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10873725	0.85[AFR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11161676	0.89[ASN][1000 genomes]
rs11161677	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11161678	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11161684	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11161685	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11161686	0.86[AFR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11161687	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11579570	0.92[ASN][1000 genomes]
rs11590890	0.92[ASN][1000 genomes]
rs12077825	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12088004	0.86[AFR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12091583	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12098168	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12119620	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12128605	0.92[ASN][1000 genomes]
rs12145864	0.84[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs12727784	0.92[ASN][1000 genomes]
rs12727916	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12735553	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12745753	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12746325	0.92[ASN][1000 genomes]
rs12753056	0.92[ASN][1000 genomes]
rs12760458	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1325260	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1481199	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1842579	0.85[AFR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2297744	0.82[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs4912437	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4912446	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6576790	0.84[AFR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6576791	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6576792	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6677315	0.84[AFR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6693669	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6697619	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6698139	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6698633	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7539262	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv582235	chr2:76881210-76997763	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1002822	chr2:76885103-76940701	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1010119	chr2:76904730-76949552	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1003119	chr2:76914457-76949552	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	n/a	n/a	inside rSNPs	diseases
5	nsv1003325	chr2:76914457-76957491	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
6	nsv998226	chr2:76919605-76949552	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription	n/a	n/a	inside rSNPs	diseases
7	nsv1002481	chr2:76919605-76957491	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
8	nsv1012020	chr2:76921092-76946538	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription	n/a	n/a	inside rSNPs	diseases
9	nsv1011976	chr2:76921664-76949315	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription	n/a	n/a	inside rSNPs	diseases
10	nsv1001059	chr2:76921664-76949552	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
11	nsv1009416	chr2:76924371-76949315	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS	n/a	n/a	inside rSNPs	diseases
12	nsv1009850	chr2:76924371-76949552	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	n/a	n/a	inside rSNPs	diseases
13	nsv1008460	chr2:76928121-76949552	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
14	nsv1013202	chr2:76928121-76956494	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
15	nsv999909	chr2:76928121-76957491	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	inside rSNPs	diseases
16	nsv582237	chr2:76929095-76949101	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
17	nsv582238	chr2:76929095-76949315	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
18	nsv874318	chr2:76929095-76956302	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76928400-76934800	Weak transcription	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links