Variant report

Variant	rs10501359
Chromosome Location	chr11:56704042-56704043
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11228836	0.82[ASN][1000 genomes]
rs11603620	0.87[ASN][1000 genomes]
rs11826402	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11828859	0.95[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs12272961	0.85[ASN][1000 genomes]
rs12282767	0.83[ASN][1000 genomes]
rs12416998	0.87[ASN][1000 genomes]
rs12421316	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12805799	0.85[ASN][1000 genomes]
rs1622278	0.88[ASN][1000 genomes]
rs17562197	0.84[MEX][hapmap]
rs17640885	0.85[ASN][1000 genomes]
rs1793426	0.85[ASN][1000 genomes]
rs1938753	0.82[ASN][1000 genomes]
rs1938759	0.85[ASN][1000 genomes]
rs1938760	0.85[ASN][1000 genomes]
rs57532445	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61886697	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61886713	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61886714	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61886716	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61886717	0.89[ASN][1000 genomes]
rs68039795	0.81[ASN][1000 genomes]
rs7118645	0.85[ASN][1000 genomes]
rs7119402	0.87[ASN][1000 genomes]
rs7128878	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs731744	0.82[ASN][1000 genomes]
rs737368	0.85[ASN][1000 genomes]
rs7938560	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7940288	0.82[ASN][1000 genomes]
rs7943283	0.82[ASN][1000 genomes]
rs7947879	0.85[ASN][1000 genomes]
rs947805	0.85[ASN][1000 genomes]
rs947806	0.81[ASN][1000 genomes]
rs950120	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9666190	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv468577	chr11:56503728-56704042	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv555101	chr11:56503728-56704042	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
3	nsv469960	chr11:56605222-56704042	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1045889	chr11:56624365-56737435	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv520375	chr11:56669830-56704042	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs10501359	TNKS1BP1	cis	cerebellum	SCAN
rs10501359	MS4A4A	cis	parietal	SCAN
rs10501359	OR4S2	cis	parietal	SCAN
rs10501359	OR5D13	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56701200-56704600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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