Variant report

Variant	rs4568383
Chromosome Location	chr5:97463948-97463949
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10463220	0.84[ASN][1000 genomes]
rs10780129	0.92[ASN][1000 genomes]
rs11135555	0.93[ASN][1000 genomes]
rs11949977	0.93[ASN][1000 genomes]
rs11952918	0.94[ASN][1000 genomes]
rs11954940	0.92[ASN][1000 genomes]
rs11958422	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11959979	0.93[ASN][1000 genomes]
rs12054950	0.92[ASN][1000 genomes]
rs12054991	0.92[ASN][1000 genomes]
rs12055020	0.97[ASN][1000 genomes]
rs12055021	0.94[ASN][1000 genomes]
rs12152744	0.92[ASN][1000 genomes]
rs12187950	0.86[ASN][1000 genomes]
rs12518775	0.95[ASN][1000 genomes]
rs12518828	0.95[ASN][1000 genomes]
rs12519976	0.94[ASN][1000 genomes]
rs12521115	0.96[ASN][1000 genomes]
rs12522700	0.97[ASN][1000 genomes]
rs13153742	0.92[ASN][1000 genomes]
rs13160494	0.99[ASN][1000 genomes]
rs13161468	0.91[ASN][1000 genomes]
rs13164386	0.83[ASN][1000 genomes]
rs13164704	0.98[ASN][1000 genomes]
rs13165935	0.94[ASN][1000 genomes]
rs13167083	0.95[ASN][1000 genomes]
rs13169480	0.93[ASN][1000 genomes]
rs13170130	0.93[ASN][1000 genomes]
rs13170158	0.92[ASN][1000 genomes]
rs13173096	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13176164	0.94[ASN][1000 genomes]
rs13177602	0.95[ASN][1000 genomes]
rs13183310	0.99[ASN][1000 genomes]
rs13189646	0.93[ASN][1000 genomes]
rs13435922	0.89[ASN][1000 genomes]
rs1421792	0.97[ASN][1000 genomes]
rs1421801	0.92[ASN][1000 genomes]
rs1559054	0.97[ASN][1000 genomes]
rs28856893	0.92[ASN][1000 genomes]
rs34475810	0.96[ASN][1000 genomes]
rs34877619	0.95[ASN][1000 genomes]
rs34879112	0.96[ASN][1000 genomes]
rs35046359	0.95[ASN][1000 genomes]
rs35541202	0.95[ASN][1000 genomes]
rs4130666	0.93[ASN][1000 genomes]
rs4266428	0.99[ASN][1000 genomes]
rs4308501	0.99[ASN][1000 genomes]
rs4311441	0.98[ASN][1000 genomes]
rs4327613	0.96[ASN][1000 genomes]
rs4351171	0.91[ASN][1000 genomes]
rs4355548	0.99[ASN][1000 genomes]
rs4394149	0.93[ASN][1000 genomes]
rs4394150	0.89[ASN][1000 genomes]
rs4404701	0.96[ASN][1000 genomes]
rs4410662	0.93[ASN][1000 genomes]
rs4422551	0.82[ASN][1000 genomes]
rs4472284	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4495209	0.93[ASN][1000 genomes]
rs4499856	0.92[ASN][1000 genomes]
rs4530782	0.94[ASN][1000 genomes]
rs4540203	0.93[ASN][1000 genomes]
rs4560566	0.93[ASN][1000 genomes]
rs4565235	0.81[ASN][1000 genomes]
rs4613742	0.95[ASN][1000 genomes]
rs4869398	0.93[ASN][1000 genomes]
rs56128630	0.95[ASN][1000 genomes]
rs58752841	0.94[ASN][1000 genomes]
rs59633134	0.95[ASN][1000 genomes]
rs60356324	0.95[ASN][1000 genomes]
rs6557041	0.83[ASN][1000 genomes]
rs6557042	0.91[ASN][1000 genomes]
rs6859600	0.93[ASN][1000 genomes]
rs6860939	0.91[ASN][1000 genomes]
rs6863011	0.91[ASN][1000 genomes]
rs6864087	0.85[ASN][1000 genomes]
rs6864879	0.92[ASN][1000 genomes]
rs6866050	0.88[ASN][1000 genomes]
rs6867072	0.92[ASN][1000 genomes]
rs6868704	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6870610	0.93[ASN][1000 genomes]
rs6883365	0.95[ASN][1000 genomes]
rs6884948	0.92[ASN][1000 genomes]
rs6889396	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6890059	0.82[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6890789	0.96[ASN][1000 genomes]
rs6891799	0.97[ASN][1000 genomes]
rs7443952	0.90[ASN][1000 genomes]
rs7444407	0.91[ASN][1000 genomes]
rs7445569	0.97[ASN][1000 genomes]
rs7447700	0.89[ASN][1000 genomes]
rs7720359	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882404	chr5:97281641-97638743	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1031989	chr5:97333291-97524353	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1034472	chr5:97357264-97523965	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2758004	chr5:97395508-97550089	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	esv2759357	chr5:97395508-97616089	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv599076	chr5:97423476-97478555	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv2753887	chr5:97439630-97532740	Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	esv2757123	chr5:97442526-97616089	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv1033719	chr5:97446209-97557327	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv516094	chr5:97447595-97512070	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv818359	chr5:97447595-97537837	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv818360	chr5:97447595-97557817	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97447600-97480000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:97460400-97464800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links