Variant report

Variant	rs10767971
Chromosome Location	chr11:32895664-32895665
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10488703	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.87[MKK][hapmap];0.92[ASN][1000 genomes]
rs10488704	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs10767970	0.87[CHB][hapmap]
rs10767972	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10835981	0.95[CHB][hapmap];0.98[CHD][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs10835983	0.95[ASN][1000 genomes]
rs10835989	0.91[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs11032024	0.95[ASN][1000 genomes]
rs11032025	0.87[CHB][hapmap];0.80[CHD][hapmap]
rs11032032	0.95[ASN][1000 genomes]
rs11032033	0.95[ASN][1000 genomes]
rs11032034	0.95[ASN][1000 genomes]
rs11032044	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs11032046	0.98[ASN][1000 genomes]
rs11032047	0.98[ASN][1000 genomes]
rs11821224	0.87[ASN][1000 genomes]
rs11826294	0.97[ASN][1000 genomes]
rs16923617	0.95[ASN][1000 genomes]
rs197705	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs197707	0.91[ASN][1000 genomes]
rs197710	0.90[ASN][1000 genomes]
rs2664692	0.89[ASN][1000 genomes]
rs28449959	0.89[ASN][1000 genomes]
rs2900981	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4755454	0.92[ASN][1000 genomes]
rs4756329	0.87[CHB][hapmap]
rs55744018	0.89[ASN][1000 genomes]
rs55763432	0.94[ASN][1000 genomes]
rs56230223	0.89[ASN][1000 genomes]
rs60475066	0.94[ASN][1000 genomes]
rs60529855	0.88[ASN][1000 genomes]
rs7118630	0.98[ASN][1000 genomes]
rs7122029	0.88[ASN][1000 genomes]
rs7122130	0.88[ASN][1000 genomes]
rs72899241	0.88[ASN][1000 genomes]
rs72899242	0.94[ASN][1000 genomes]
rs72901219	0.98[ASN][1000 genomes]
rs72901225	0.95[ASN][1000 genomes]
rs72901227	0.95[ASN][1000 genomes]
rs7933966	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.91[MKK][hapmap];0.97[ASN][1000 genomes]
rs7943715	0.90[ASN][1000 genomes]
rs7944652	0.87[CHB][hapmap]
rs956322	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.87[MKK][hapmap];0.96[ASN][1000 genomes]
rs9943603	0.99[ASN][1000 genomes]
rs9943661	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758262	chr11:32714643-33049940	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	esv2759815	chr11:32714643-33049940	Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
3	esv2757434	chr11:32792784-32958609	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	esv34742	chr11:32796092-33004024	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
5	esv2753057	chr11:32796124-33061724	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
6	esv2753743	chr11:32796124-33084924	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
7	nsv897190	chr11:32801921-32951836	Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
8	nsv897191	chr11:32805169-32903263	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	nsv897192	chr11:32828760-32903263	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv897193	chr11:32838288-32903263	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Parkinson's disease (age of onset)	19772629	GWAS catalog

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs10767971	QSER1	cis	cerebellum	SCAN
rs10767971	QSER1	cis	parietal	SCAN
rs10767971	FSHB	cis	parietal	SCAN

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32895400-32896000	Enhancers	A549	lung
2	chr11:32895400-32896200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr11:32895400-32896200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr11:32895600-32896000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:32895600-32896200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr11:32895600-32896200	Enhancers	Hela-S3	cervix
7	chr11:32895600-32896400	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links