Variant report

Variant	rs1455432
Chromosome Location	chr5:97734875-97734876
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10035546	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10036788	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10036839	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10050404	1.00[CEU][hapmap]
rs10050543	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10054643	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10073933	0.82[EUR][1000 genomes]
rs10076590	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11950953	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11953877	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11953894	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11954911	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11955115	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11955987	0.82[EUR][1000 genomes]
rs11959995	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12516014	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12516667	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12517476	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12519087	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12520566	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12523434	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1455424	0.89[ASN][1000 genomes]
rs1455425	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1455426	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.88[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17165878	0.82[EUR][1000 genomes]
rs17165943	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35382921	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4702968	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4702970	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4703066	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4703070	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4703347	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4703354	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59277777	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59423561	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60249733	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61740530	0.86[EUR][1000 genomes]
rs62369875	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6594645	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6594647	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6596727	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs6596748	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6862206	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6863762	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs6870895	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6872708	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6872831	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6877032	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6885408	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6890493	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73143833	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73159220	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73159222	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73159223	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73159226	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73159258	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7702659	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7702702	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7714842	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7715004	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7734263	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7734271	1.00[EUR][1000 genomes];1.00[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	nsv882407	chr5:97553255-97783046	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv882408	chr5:97616089-97836794	Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv830419	chr5:97653713-97829079	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv4928	chr5:97689980-97734899	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1018555	chr5:97719032-97873906	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 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	chr5:97732600-97735000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:97733200-97735200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:97733400-97737200	Weak transcription	Osteobl	bone
4	chr5:97733800-97737000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr5:97734000-97736800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:97734400-97738600	Weak transcription	Brain Anterior Caudate	brain
7	chr5:97734600-97736600	Weak transcription	NHDF-Ad	bronchial
8	chr5:97734800-97735200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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