Variant report

Variant	rs11739338
Chromosome Location	chr5:41301337-41301338
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10462017	0.85[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs10512774	0.85[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs10512775	0.84[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs11737958	0.95[CHB][hapmap];0.92[CHD][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs11739235	0.84[ASN][1000 genomes]
rs11739372	0.84[ASN][1000 genomes]
rs11739553	0.89[ASW][hapmap];1.00[CEU][hapmap];0.85[CHB][hapmap];0.92[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];0.85[LWK][hapmap];0.85[MEX][hapmap];0.97[TSI][hapmap];0.85[YRI][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11739969	0.84[ASN][1000 genomes]
rs11740787	0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs11741144	0.84[ASN][1000 genomes]
rs11741795	0.81[ASN][1000 genomes]
rs11744499	0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap];0.89[ASN][1000 genomes]
rs11747859	0.85[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs1373639	0.95[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs1423312	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1460953	0.85[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs16871219	0.85[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs16871220	0.85[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs16871222	0.85[CHB][hapmap];0.92[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs16871258	0.85[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs16871269	0.85[CHB][hapmap];0.92[CHD][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs1822820	1.00[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1904178	0.85[CHB][hapmap];0.92[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs1904179	0.84[ASN][1000 genomes]
rs2054445	0.85[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs2161542	0.85[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs2197422	1.00[CEU][hapmap];0.85[CHB][hapmap];0.92[CHD][hapmap];0.80[GIH][hapmap];0.95[JPT][hapmap];0.85[MEX][hapmap];0.97[TSI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2329601	0.84[ASN][1000 genomes]
rs2329602	0.85[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs2329604	0.85[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs2329671	0.85[CHB][hapmap];0.92[CHD][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs2860000	0.85[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs318837	0.86[CEU][hapmap]
rs318842	0.86[CEU][hapmap]
rs4245978	0.84[ASN][1000 genomes]
rs4957153	0.85[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs4957389	0.84[ASN][1000 genomes]
rs4957390	0.81[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs4957391	0.84[ASN][1000 genomes]
rs4957392	0.84[ASN][1000 genomes]
rs60271243	0.92[ASN][1000 genomes]
rs60917374	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61282403	0.84[ASN][1000 genomes]
rs67043243	0.84[ASN][1000 genomes]
rs6872806	1.00[CEU][hapmap];0.85[CHB][hapmap];0.92[CHD][hapmap];0.95[JPT][hapmap];0.97[TSI][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6886372	0.84[ASN][1000 genomes]
rs6886899	0.84[ASN][1000 genomes]
rs6898606	1.00[CEU][hapmap];0.85[CHB][hapmap];0.90[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.97[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72755961	0.84[ASN][1000 genomes]
rs72755967	0.84[ASN][1000 genomes]
rs72755968	0.84[ASN][1000 genomes]
rs72755970	0.84[ASN][1000 genomes]
rs72755972	0.84[ASN][1000 genomes]
rs72755973	0.84[ASN][1000 genomes]
rs72755982	0.85[ASN][1000 genomes]
rs72755983	0.84[ASN][1000 genomes]
rs72755984	0.85[ASN][1000 genomes]
rs73075962	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs765176	0.85[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs765177	0.85[CHB][hapmap];0.92[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs7701760	0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs7703589	0.85[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs7704046	0.85[CHB][hapmap];0.92[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs7723649	0.84[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs7724627	0.87[ASN][1000 genomes]
rs7725517	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7727658	0.85[CHB][hapmap];0.87[CHD][hapmap];0.84[ASN][1000 genomes]
rs7729454	0.85[CHB][hapmap];0.92[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs7735604	0.84[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs978727	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427717	chr5:41201377-41369202	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv830269	chr5:41209113-41393536	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41299400-41304800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:41300000-41307000	Weak transcription	Aorta	Aorta
3	chr5:41301000-41302000	Weak transcription	Fetal Heart	heart

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