Variant report

Variant	rs9598274
Chromosome Location	chr13:61994491-61994492
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs4277248	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4499128	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6562178	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7325869	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8002097	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9528340	0.92[EUR][1000 genomes]
rs9539174	0.92[EUR][1000 genomes]
rs9539176	0.96[CEU][hapmap];0.84[CHB][hapmap];0.81[JPT][hapmap];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9539177	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9539178	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9539187	0.80[ASN][1000 genomes]
rs9563920	0.95[CEU][hapmap];0.82[CHB][hapmap];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9563921	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9563922	0.94[JPT][hapmap];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9563923	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9563924	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9563925	0.96[CEU][hapmap];0.84[CHB][hapmap];0.81[JPT][hapmap];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9570582	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9570584	0.90[CEU][hapmap];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9570585	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9570586	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9570587	0.96[CEU][hapmap];0.83[CHB][hapmap];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9570588	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9570589	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9570590	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9570591	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9570593	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900245	chr13:61873379-62057698	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv948661	chr13:61906251-62179649	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv2761266	chr13:61928642-62690828	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv832628	chr13:61985540-62153692	Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61990200-61994800	Weak transcription	Fetal Heart	heart

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