Variant report

Variant	rs332531
Chromosome Location	chr5:90790451-90790452
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10041402	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10045280	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10052492	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10054820	0.83[EUR][1000 genomes]
rs10058025	0.94[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.80[EUR][1000 genomes]
rs10059163	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10063683	0.94[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.80[EUR][1000 genomes]
rs10073657	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10073935	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1035476	0.82[EUR][1000 genomes]
rs1035477	0.83[EUR][1000 genomes]
rs10474352	0.81[CHB][hapmap];0.82[EUR][1000 genomes]
rs10474353	0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10942634	0.85[AMR][1000 genomes]
rs11950530	0.94[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.80[EUR][1000 genomes]
rs11959525	0.94[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap];0.80[EUR][1000 genomes]
rs12110065	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12110303	0.84[AMR][1000 genomes]
rs12188467	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12651840	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12654787	0.94[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.80[EUR][1000 genomes]
rs12655973	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12656350	0.83[EUR][1000 genomes]
rs1363839	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes]
rs1477348	0.80[EUR][1000 genomes]
rs1477349	0.80[EUR][1000 genomes]
rs186717	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1895448	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1895449	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1964292	0.86[EUR][1000 genomes]
rs1966494	0.88[AMR][1000 genomes]
rs2004483	0.82[EUR][1000 genomes]
rs2052553	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2059207	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2059208	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2367353	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2367526	0.81[EUR][1000 genomes]
rs2839728	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2887007	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs332529	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs332544	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4382199	0.83[EUR][1000 genomes]
rs60513756	0.82[EUR][1000 genomes]
rs6452951	0.84[AMR][1000 genomes]
rs6452953	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6452954	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs66759971	0.82[EUR][1000 genomes]
rs6860948	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6865495	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6866191	0.83[EUR][1000 genomes]
rs6866923	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes]
rs6867091	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6869717	0.80[EUR][1000 genomes]
rs6882269	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs746637	0.94[CEU][hapmap];0.91[CHB][hapmap]
rs7708782	0.94[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.82[EUR][1000 genomes]
rs7715402	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7718871	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes]
rs7720132	0.94[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.82[EUR][1000 genomes]
rs889213	0.94[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap]
rs9293568	0.83[EUR][1000 genomes]
rs9686361	0.83[EUR][1000 genomes]
rs985434	0.94[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.83[EUR][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	nsv1024813	chr5:90321535-90870739	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
2	nsv537806	chr5:90321535-90870739	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
3	nsv1030453	chr5:90709080-90849693	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3414088	chr5:90744553-90861592	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90789200-90790600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr5:90789200-90790800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr5:90789200-90801400	Weak transcription	Aorta	Aorta
4	chr5:90790400-90790600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:90790400-90790600	Enhancers	GM12878-XiMat	blood
6	chr5:90790400-90790800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr5:90790400-90791800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:90790400-90791800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr5:90790400-90792000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr5:90790400-90792000	Enhancers	HUES48 Cell Line	embryonic stem cell

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