Variant report

Variant	rs7111174
Chromosome Location	chr11:92968895-92968896
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:92967004..92969255-chr11:93384967..93385922,6	K562	blood:
2	chr11:92966947..92969391-chr11:93461362..93463469,2	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10830987	0.84[AMR][1000 genomes]
rs10830995	0.87[CHB][hapmap]
rs10830997	0.82[CHB][hapmap]
rs10831000	0.84[AMR][1000 genomes]
rs10831001	0.87[CHB][hapmap]
rs10831002	0.88[CHB][hapmap]
rs11020180	0.84[AMR][1000 genomes]
rs11020183	0.87[CHB][hapmap]
rs11020190	0.87[CHB][hapmap]
rs11020191	0.84[AMR][1000 genomes]
rs11020196	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11020197	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11020198	0.83[ASN][1000 genomes]
rs11020199	0.87[ASN][1000 genomes]
rs11020200	0.87[ASN][1000 genomes]
rs11020206	0.84[ASN][1000 genomes]
rs11020207	0.95[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11020208	0.90[ASN][1000 genomes]
rs12221889	0.84[AMR][1000 genomes]
rs12365990	0.87[CHB][hapmap];0.84[AMR][1000 genomes]
rs1446915	0.97[ASN][1000 genomes]
rs1446916	0.94[ASN][1000 genomes]
rs16918625	0.87[CHB][hapmap]
rs16918677	0.95[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2121467	0.87[CHB][hapmap];0.84[AMR][1000 genomes]
rs2399605	0.87[ASN][1000 genomes]
rs3943572	0.87[CHB][hapmap]
rs3957618	0.88[CHB][hapmap];0.84[AMR][1000 genomes]
rs4753437	0.87[CHB][hapmap];0.84[ASN][1000 genomes]
rs4753438	0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4753439	0.87[ASN][1000 genomes]
rs58121936	0.95[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs66763553	0.85[ASN][1000 genomes]
rs7121033	0.89[ASN][1000 genomes]
rs7121713	0.86[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs7933585	0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7933922	0.87[ASN][1000 genomes]
rs7936669	0.84[ASN][1000 genomes]
rs7936931	0.87[ASN][1000 genomes]
rs935447	0.87[CHB][hapmap];0.83[ASN][1000 genomes]
rs935448	0.86[CHB][hapmap];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039134	chr11:92790000-93219942	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv898177	chr11:92877533-92971874	Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv436	chr11:92967000-92985674	Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv514640	chr11:92967440-92972784	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv3464353	chr11:92967896-92972804	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv3464331	chr11:92967903-92972689	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv3464342	chr11:92967919-92972744	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv826034	chr11:92967982-92972677	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv826035	chr11:92967982-92972713	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv3464364	chr11:92968000-92972695	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv498765	chr11:92968001-92972695	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 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
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