Variant report

Variant	rs4711858
Chromosome Location	chr6:12880131-12880132
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10948235	1.00[CHB][hapmap]
rs10948244	1.00[CHB][hapmap]
rs10948247	1.00[CHB][hapmap]
rs12523719	1.00[CHB][hapmap]
rs12526453	1.00[JPT][hapmap]
rs12528956	1.00[CHB][hapmap]
rs12530250	1.00[JPT][hapmap]
rs13201878	1.00[JPT][hapmap]
rs13217579	1.00[CHB][hapmap]
rs1332840	1.00[CHB][hapmap]
rs1332841	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1360579	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1412740	1.00[CHB][hapmap]
rs1412741	1.00[CHB][hapmap]
rs1412744	0.91[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1412751	1.00[CHB][hapmap]
rs1412752	1.00[CHB][hapmap]
rs1412753	1.00[CHB][hapmap]
rs1572000	1.00[CHB][hapmap]
rs1572002	1.00[CHB][hapmap]
rs17617207	1.00[CHB][hapmap]
rs17679417	1.00[CHB][hapmap]
rs17679501	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1953089	1.00[CHB][hapmap]
rs2327619	1.00[CHB][hapmap]
rs4131857	1.00[JPT][hapmap]
rs4331981	1.00[JPT][hapmap]
rs4711857	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4714866	1.00[CHB][hapmap]
rs4714870	1.00[CHB][hapmap]
rs4714946	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59402659	0.83[AFR][1000 genomes]
rs6458461	1.00[CHB][hapmap]
rs6458503	1.00[CHB][hapmap]
rs66867947	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6909834	1.00[CHB][hapmap]
rs6916334	1.00[CHB][hapmap]
rs6917493	1.00[CHB][hapmap]
rs6924150	1.00[CHB][hapmap]
rs6938417	1.00[CHB][hapmap]
rs6941422	1.00[CHB][hapmap]
rs6941624	1.00[CHB][hapmap]
rs7739181	1.00[JPT][hapmap]
rs7748950	1.00[CHB][hapmap]
rs7757205	1.00[CHB][hapmap]
rs7757858	1.00[CHB][hapmap]
rs7760140	1.00[CHB][hapmap]
rs7760286	1.00[CHB][hapmap]
rs7770745	1.00[CHB][hapmap]
rs7771962	1.00[CHB][hapmap];0.83[AFR][1000 genomes]
rs7775901	1.00[JPT][hapmap]
rs7776079	1.00[CHB][hapmap]
rs883947	1.00[CHB][hapmap]
rs9296464	1.00[CHB][hapmap]
rs9296494	1.00[CHB][hapmap]
rs9395190	1.00[CHB][hapmap]
rs944766	1.00[CHB][hapmap]
rs944767	1.00[CHB][hapmap]
rs9463106	1.00[CHB][hapmap]
rs9463110	1.00[CHB][hapmap]
rs9463134	1.00[CHB][hapmap]
rs9472551	1.00[CHB][hapmap]
rs9472777	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9472786	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9473086	1.00[JPT][hapmap]
rs950720	1.00[CHB][hapmap]

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	esv3521000	chr6:12561306-13128519	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3521001	chr6:12561306-13128519	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv830587	chr6:12769661-12939875	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv830588	chr6:12793530-12972493	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:12867400-12887600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:12867600-12886800	Weak transcription	Brain Anterior Caudate	brain
3	chr6:12870400-12885200	Weak transcription	Brain Germinal Matrix	brain
4	chr6:12875400-12885200	Weak transcription	Fetal Brain Female	brain
5	chr6:12876200-12881400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:12877400-12881200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr6:12877600-12881200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:12877600-12881200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr6:12877600-12881400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr6:12877600-12881600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr6:12878000-12880600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr6:12878600-12880600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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