Variant report

Variant	rs4705038
Chromosome Location	chr5:146733598-146733599
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10039739	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10040325	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10041697	1.00[CHB][hapmap];0.82[JPT][hapmap];0.99[ASN][1000 genomes]
rs10041912	0.90[CHB][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10059609	0.92[ASN][1000 genomes]
rs10065264	0.82[ASN][1000 genomes]
rs10070932	0.84[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10077515	0.84[CEU][hapmap];0.99[EUR][1000 genomes]
rs10079191	1.00[CHB][hapmap];0.82[JPT][hapmap];0.99[ASN][1000 genomes]
rs10079272	1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10477336	0.91[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10515580	0.91[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11747533	0.92[ASN][1000 genomes]
rs11748615	0.91[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11951154	0.91[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11954258	0.91[CEU][hapmap];0.94[EUR][1000 genomes]
rs11954789	1.00[CHB][hapmap];0.96[ASN][1000 genomes]
rs11955235	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12332485	1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12514269	1.00[CHB][hapmap];0.82[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12659468	0.92[CEU][hapmap];0.95[CHB][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13170279	1.00[CHB][hapmap];0.82[JPT][hapmap];0.99[ASN][1000 genomes]
rs1364371	0.92[CEU][hapmap];0.93[EUR][1000 genomes]
rs1424293	0.89[CHB][hapmap];0.82[ASN][1000 genomes]
rs17106458	1.00[CHB][hapmap];0.96[ASN][1000 genomes]
rs17106505	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17547843	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs1834122	0.92[ASN][1000 genomes]
rs1895565	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2400294	0.81[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2400295	0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4705163	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4705164	0.84[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4705165	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4705166	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57921061	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62377743	0.94[EUR][1000 genomes]
rs62379566	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs6866098	1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6867255	0.92[ASN][1000 genomes]
rs6872292	0.92[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6884181	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs6891535	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs72831382	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7707452	0.89[CHB][hapmap];0.92[ASN][1000 genomes]
rs918797	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs918798	0.91[CEU][hapmap];0.94[CHB][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9885145	1.00[CHB][hapmap];0.82[JPT][hapmap];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015804	chr5:146066000-146788233	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv537915	chr5:146066000-146788233	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv519847	chr5:146166378-146812647	Bivalent/Poised TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv599938	chr5:146169511-146806365	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv869238	chr5:146179403-146787986	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:146727600-146743000	Weak transcription	Aorta	Aorta
2	chr5:146728600-146733800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:146729200-146743000	Weak transcription	Brain Substantia Nigra	brain
4	chr5:146730400-146737000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:146732800-146733800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:146732800-146740200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr5:146733400-146733800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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