Variant report

Variant	rs10077515
Chromosome Location	chr5:146725558-146725559
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10039739	0.97[EUR][1000 genomes]
rs10040325	0.99[EUR][1000 genomes]
rs10041912	0.97[EUR][1000 genomes]
rs10054226	1.00[JPT][hapmap]
rs10064995	0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10070932	0.84[CEU][hapmap];0.95[EUR][1000 genomes]
rs10477336	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs10515580	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs11741401	0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11742132	0.85[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11748615	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs11951154	0.97[EUR][1000 genomes]
rs11954258	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11955126	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11955235	0.97[EUR][1000 genomes]
rs12054990	0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12055338	0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12514269	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs12659468	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs1364371	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17106505	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17547843	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17548011	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs1895565	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2400294	0.82[CEU][hapmap];0.94[EUR][1000 genomes]
rs2400295	0.92[CEU][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4705038	0.84[CEU][hapmap];0.99[EUR][1000 genomes]
rs4705163	0.95[EUR][1000 genomes]
rs4705164	1.00[CEU][hapmap];0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4705165	0.84[CEU][hapmap];1.00[EUR][1000 genomes]
rs4705166	0.84[CEU][hapmap];0.93[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs57921061	0.97[EUR][1000 genomes]
rs62377743	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62379566	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6872292	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs6891535	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72831382	0.95[EUR][1000 genomes]
rs7710326	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs918797	0.92[CEU][hapmap];0.98[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs918798	0.92[CEU][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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
6	esv2763507	chr5:146718961-146727485	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:146707600-146725600	Weak transcription	Pancreas	Pancrea
2	chr5:146721800-146726600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr5:146722200-146727000	Weak transcription	Aorta	Aorta
4	chr5:146723000-146727000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:146723000-146733400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr5:146724200-146725600	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr5:146725200-146725800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:146725400-146726800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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