Variant report

Variant	rs56782837
Chromosome Location	chr3:98029025-98029026
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1121369	0.86[ASN][1000 genomes]
rs1497546	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55800540	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55817294	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55836250	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55848866	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56115538	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56186058	0.96[EUR][1000 genomes]
rs56331876	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56347336	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56908826	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58784693	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59191375	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59949657	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60249448	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60896887	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61196885	0.86[ASN][1000 genomes]
rs61310789	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61483213	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61578197	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267259	0.86[ASN][1000 genomes]
rs62267361	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267362	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267365	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62267366	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267368	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267373	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267374	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267375	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267376	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267377	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267379	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62268282	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62268291	0.96[EUR][1000 genomes]
rs62268860	0.86[ASN][1000 genomes]
rs62268890	0.86[ASN][1000 genomes]
rs62268895	0.86[ASN][1000 genomes]
rs62268917	0.80[ASN][1000 genomes]
rs62268918	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62268930	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62270682	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62270685	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6786806	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72937135	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7628736	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7640176	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869347	chr3:97742604-98051633	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv877209	chr3:97806616-98049409	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv963576	chr3:97825434-98041343	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1004820	chr3:97852875-98169488	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv834773	chr3:97855362-98043888	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1000834	chr3:97859880-98095473	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv877212	chr3:97931105-98033400	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	esv1842860	chr3:97934241-98075543	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1009918	chr3:97946030-98155450	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr3:98028400-98039400	Weak transcription	H9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links