Variant report

Variant	rs11942294
Chromosome Location	chr4:142517416-142517417
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10519610	1.00[JPT][hapmap]
rs11100721	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1114714	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11930959	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12152590	0.90[ASN][1000 genomes]
rs12498901	1.00[JPT][hapmap]
rs12504148	1.00[JPT][hapmap]
rs12510514	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12513220	0.90[ASN][1000 genomes]
rs12643182	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13106515	0.90[ASN][1000 genomes]
rs13117878	0.90[GIH][hapmap]
rs13120181	0.87[ASN][1000 genomes]
rs13127492	0.90[ASN][1000 genomes]
rs13132563	0.87[ASN][1000 genomes]
rs13133830	0.90[ASN][1000 genomes]
rs13142400	0.93[ASN][1000 genomes]
rs1607595	1.00[JPT][hapmap]
rs17362224	0.90[ASN][1000 genomes]
rs17364630	1.00[JPT][hapmap]
rs1850852	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1949668	0.90[ASN][1000 genomes]
rs1949669	0.90[ASN][1000 genomes]
rs2049181	0.90[ASN][1000 genomes]
rs2139992	0.87[ASN][1000 genomes]
rs34124780	0.90[ASN][1000 genomes]
rs34149126	0.90[ASN][1000 genomes]
rs34274316	0.90[ASN][1000 genomes]
rs34579838	0.90[ASN][1000 genomes]
rs34899172	0.90[ASN][1000 genomes]
rs34962680	0.93[ASN][1000 genomes]
rs35308689	0.90[ASN][1000 genomes]
rs35316642	0.80[ASN][1000 genomes]
rs35372192	0.90[ASN][1000 genomes]
rs35969143	0.90[ASN][1000 genomes]
rs36043894	0.93[ASN][1000 genomes]
rs36124988	0.90[ASN][1000 genomes]
rs4519867	0.87[ASN][1000 genomes]
rs4956405	1.00[JPT][hapmap]
rs56200104	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58474929	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62326618	0.90[ASN][1000 genomes]
rs62326619	0.90[ASN][1000 genomes]
rs62327371	0.90[ASN][1000 genomes]
rs62327372	0.90[ASN][1000 genomes]
rs62327373	0.87[ASN][1000 genomes]
rs62327375	0.93[ASN][1000 genomes]
rs62327376	0.93[ASN][1000 genomes]
rs62327381	0.93[ASN][1000 genomes]
rs67407219	0.87[ASN][1000 genomes]
rs6812199	0.87[ASN][1000 genomes]
rs6814497	0.87[ASN][1000 genomes]
rs6830391	0.87[ASN][1000 genomes]
rs6837886	0.84[ASN][1000 genomes]
rs6841939	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6842735	1.00[JPT][hapmap]
rs6850492	1.00[JPT][hapmap]
rs72728300	0.87[ASN][1000 genomes]
rs72730041	0.84[ASN][1000 genomes]
rs7349640	1.00[JPT][hapmap]
rs7668761	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7671458	1.00[JPT][hapmap]
rs7683697	0.88[EUR][1000 genomes]
rs7692755	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880172	chr4:142355535-142565089	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv880173	chr4:142355535-142666106	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830094	chr4:142411738-142567788	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv3401979	chr4:142434442-142803321	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1018949	chr4:142451823-142732365	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1030822	chr4:142487721-142706053	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1027004	chr4:142487721-143007320	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv498005	chr4:142515689-143502988	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr4:142517200-142517600	Enhancers	Muscle Satellite Cultured Cells	--
2	chr4:142517200-142518000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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