Variant report

Variant	rs10836452
Chromosome Location	chr11:4694428-4694429
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10768164	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10768165	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10768166	0.83[ASN][1000 genomes]
rs10768168	0.92[ASN][1000 genomes]
rs10836440	0.83[ASN][1000 genomes]
rs10836441	0.83[ASN][1000 genomes]
rs10836445	0.83[ASN][1000 genomes]
rs10836446	0.83[ASN][1000 genomes]
rs10836447	0.83[ASN][1000 genomes]
rs10836448	0.83[ASN][1000 genomes]
rs10836449	0.83[ASN][1000 genomes]
rs10836451	0.82[ASN][1000 genomes]
rs11033251	0.90[CHB][hapmap];0.86[CHD][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs11033253	0.85[ASN][1000 genomes]
rs11033255	0.83[ASN][1000 genomes]
rs11033264	0.83[ASN][1000 genomes]
rs11033271	0.83[ASN][1000 genomes]
rs11033272	0.83[ASN][1000 genomes]
rs11033275	0.85[ASN][1000 genomes]
rs11033277	0.82[ASN][1000 genomes]
rs11033278	0.83[ASN][1000 genomes]
rs11033281	0.83[ASN][1000 genomes]
rs12363886	0.81[ASN][1000 genomes]
rs12417964	0.83[ASN][1000 genomes]
rs12421856	0.83[ASN][1000 genomes]
rs17225636	0.83[ASN][1000 genomes]
rs1995562	0.83[ASN][1000 genomes]
rs2201337	0.83[ASN][1000 genomes]
rs4910662	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58150027	0.83[ASN][1000 genomes]
rs6578511	0.90[CHB][hapmap];0.81[JPT][hapmap];0.84[ASN][1000 genomes]
rs6578512	0.85[CHB][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs6578513	0.83[ASN][1000 genomes]
rs6578514	0.85[ASN][1000 genomes]
rs6578516	0.83[ASN][1000 genomes]
rs6578517	0.83[ASN][1000 genomes]
rs6578518	0.83[ASN][1000 genomes]
rs7113772	0.85[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs7115827	0.85[CHB][hapmap];0.81[CHD][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs7117050	0.89[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs7124096	0.83[ASN][1000 genomes]
rs7124760	0.85[CHB][hapmap];0.83[CHD][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs72865852	0.83[ASN][1000 genomes]
rs72865853	0.83[ASN][1000 genomes]
rs72865854	0.82[ASN][1000 genomes]
rs72865864	0.83[ASN][1000 genomes]
rs7924588	0.83[ASN][1000 genomes]
rs7934446	0.85[ASN][1000 genomes]
rs7936442	0.81[ASN][1000 genomes]
rs7949117	0.87[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	nsv1043803	chr11:4388448-4837042	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
2	nsv540916	chr11:4388448-4837042	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
3	nsv1048224	chr11:4390227-4920324	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
4	nsv540917	chr11:4390227-4920324	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
5	nsv896911	chr11:4400801-4806872	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
6	nsv832055	chr11:4550894-4736340	Strong transcription Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	esv3424302	chr11:4585155-4880050	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
8	nsv1054847	chr11:4642875-5200656	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
9	nsv896915	chr11:4659419-4844393	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
10	nsv832056	chr11:4673001-4824890	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs10836452	CEND1	cis	parietal	SCAN
rs10836452	CARS	cis	cerebellum	SCAN
rs10836452	KCNQ1	cis	parietal	SCAN
rs10836452	NUP98	cis	cerebellum	SCAN

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4693000-4694600	Enhancers	Fetal Heart	heart
2	chr11:4693200-4694600	Enhancers	HSMMtube	muscle
3	chr11:4693200-4696000	Enhancers	NHDF-Ad	bronchial
4	chr11:4693400-4694600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr11:4693400-4694600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr11:4693400-4694600	Enhancers	Rectal Smooth Muscle	rectum
7	chr11:4693800-4694600	Enhancers	Colon Smooth Muscle	Colon
8	chr11:4694400-4694600	Enhancers	Fetal Kidney	kidney

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