Variant report

Variant	rs10232941
Chromosome Location	chr7:27456002-27456003
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:27455758..27458549-chr7:27459040..27460885,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10252971	0.88[ASN][1000 genomes]
rs10268859	0.99[ASN][1000 genomes]
rs10951165	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11520770	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs11563321	0.80[ASN][1000 genomes]
rs11563380	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs11563567	1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs11563971	0.81[JPT][hapmap]
rs11978918	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs12667419	0.95[ASN][1000 genomes]
rs12668112	0.89[ASN][1000 genomes]
rs12668981	0.82[AMR][1000 genomes]
rs12672272	0.99[ASN][1000 genomes]
rs17429361	0.91[CHB][hapmap]
rs17429641	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs17429648	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs17439000	0.91[CHB][hapmap]
rs17439221	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs17439235	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs17439374	0.98[ASN][1000 genomes]
rs2074336	0.97[ASN][1000 genomes]
rs2074337	0.88[ASN][1000 genomes]
rs2074338	0.88[ASN][1000 genomes]
rs2893286	0.99[ASN][1000 genomes]
rs4298409	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs4357199	0.80[CHB][hapmap]
rs4470906	1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs4529360	0.92[ASN][1000 genomes]
rs4719891	0.85[ASN][1000 genomes]
rs56294122	0.81[AMR][1000 genomes]
rs58842477	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6953463	0.87[ASN][1000 genomes]
rs6957441	1.00[CHB][hapmap];0.88[ASN][1000 genomes]
rs6957649	1.00[CHB][hapmap];0.88[ASN][1000 genomes]
rs72595217	0.81[AMR][1000 genomes]
rs7798437	0.89[ASN][1000 genomes]
rs929242	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs929243	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531024	chr7:27194426-27461954	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
2	nsv830930	chr7:27395838-27587355	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27444800-27458000	Weak transcription	Pancreas	Pancrea
2	chr7:27444800-27458000	Weak transcription	Stomach Mucosa	stomach

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