Variant report

Variant	rs7706858
Chromosome Location	chr5:74314884-74314885
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10462510	0.89[ASN][1000 genomes]
rs11955513	0.82[ASN][1000 genomes]
rs11957690	1.00[CEU][hapmap];0.85[JPT][hapmap];0.93[EUR][1000 genomes]
rs12515891	0.91[ASN][1000 genomes]
rs12516438	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12655792	0.92[CHB][hapmap]
rs12657184	0.92[CHB][hapmap]
rs34018438	0.96[EUR][1000 genomes]
rs3811986	1.00[CEU][hapmap];0.85[JPT][hapmap];0.94[EUR][1000 genomes]
rs3811987	1.00[CEU][hapmap];0.85[JPT][hapmap];0.94[EUR][1000 genomes]
rs4285200	0.95[CEU][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4290996	0.95[CEU][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4492095	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4704166	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56682994	0.94[EUR][1000 genomes]
rs58243356	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58323964	0.89[ASN][1000 genomes]
rs59923116	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs59992473	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60661930	0.95[ASN][1000 genomes]
rs61342638	0.88[ASN][1000 genomes]
rs61616736	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62369160	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62369164	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62369166	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62369167	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62369187	0.86[ASN][1000 genomes]
rs62369188	0.85[ASN][1000 genomes]
rs6874469	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72768311	0.91[ASN][1000 genomes]
rs7725085	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7726378	0.89[EUR][1000 genomes]
rs7734055	0.85[ASN][1000 genomes]
rs7734427	1.00[CEU][hapmap];0.85[JPT][hapmap];0.93[EUR][1000 genomes]
rs7736471	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830352	chr5:74189495-74337944	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1018865	chr5:74246293-74494552	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv969994	chr5:74314591-74330479	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr5:74303600-74316000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:74313600-74318200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:74313600-74341800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:74314200-74315200	Enhancers	NHDF-Ad	bronchial
5	chr5:74314600-74315200	Enhancers	NH-A	brain
6	chr5:74314600-74324800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr5:74314800-74315800	Weak transcription	Pancreas	Pancrea

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