Variant report

Variant	rs11885804
Chromosome Location	chr2:50654677-50654678
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10187911	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs10204268	0.80[EUR][1000 genomes]
rs10210298	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs10490227	0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11125305	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11901106	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12475335	0.82[JPT][hapmap]
rs12616901	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12619946	0.82[JPT][hapmap]
rs12620185	0.92[EUR][1000 genomes]
rs13390864	0.82[JPT][hapmap]
rs13396103	0.81[JPT][hapmap]
rs13404855	1.00[CEU][hapmap]
rs13407657	0.81[JPT][hapmap]
rs1520439	0.81[JPT][hapmap]
rs17040640	0.82[JPT][hapmap]
rs17040648	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2160443	0.82[JPT][hapmap]
rs2176853	1.00[CEU][hapmap]
rs2176854	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2176855	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs35153288	0.82[AMR][1000 genomes]
rs4563262	0.83[CHB][hapmap];0.85[JPT][hapmap];0.82[AMR][1000 genomes]
rs4971557	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs4971668	0.92[EUR][1000 genomes]
rs4971678	0.81[AMR][1000 genomes]
rs5019239	1.00[CEU][hapmap]
rs6711307	0.81[JPT][hapmap]
rs6717441	0.82[JPT][hapmap]
rs6727675	0.84[EUR][1000 genomes]
rs6743117	0.82[JPT][hapmap]
rs6743584	0.82[JPT][hapmap]
rs6747128	0.82[JPT][hapmap]
rs6747258	0.82[JPT][hapmap]
rs6756081	0.86[JPT][hapmap]
rs6756479	0.82[JPT][hapmap]
rs719293	0.96[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs72878310	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73934105	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9309182	0.81[JPT][hapmap]
rs989378	0.83[CHB][hapmap]
rs9917153	0.87[CHB][hapmap];0.81[JPT][hapmap];0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492164	chr2:50399251-51029090	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1000653	chr2:50417660-51083470	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv535693	chr2:50417660-51083470	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv948548	chr2:50569117-50695100	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv948361	chr2:50611076-50785178	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv933786	chr2:50628354-50780185	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1010510	chr2:50649641-51011565	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv535694	chr2:50649641-51011565	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv961689	chr2:50654619-50658155	Enhancers Weak transcription	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	chr2:50654200-50657400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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