Variant report

Variant	rs11794203
Chromosome Location	chr9:18235969-18235970
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs11787755	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11787918	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11788211	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11788314	1.00[ASN][1000 genomes]
rs11789982	1.00[ASN][1000 genomes]
rs11790235	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11790282	1.00[ASN][1000 genomes]
rs11790387	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11790414	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11790830	1.00[ASN][1000 genomes]
rs11791252	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11794137	1.00[ASN][1000 genomes]
rs11794764	1.00[ASN][1000 genomes]
rs11794779	1.00[ASN][1000 genomes]
rs11795067	1.00[ASN][1000 genomes]
rs11795109	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11795249	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11795321	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16936468	1.00[ASN][1000 genomes]
rs17196795	1.00[ASN][1000 genomes]
rs17198051	1.00[ASN][1000 genomes]
rs17775838	1.00[ASN][1000 genomes]
rs17788716	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1944745	1.00[ASN][1000 genomes]
rs4246140	1.00[ASN][1000 genomes]
rs55678641	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55742842	1.00[ASN][1000 genomes]
rs55767089	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55768778	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55879948	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55924836	1.00[ASN][1000 genomes]
rs55941140	1.00[ASN][1000 genomes]
rs55970620	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56290103	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56316407	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59977859	1.00[ASN][1000 genomes]
rs72684909	1.00[ASN][1000 genomes]
rs72684911	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72684912	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72684932	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72684934	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72684935	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72684943	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72684944	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72684945	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72684948	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72684960	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72684967	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72684971	0.81[EUR][1000 genomes]
rs72699447	1.00[ASN][1000 genomes]
rs72699461	1.00[ASN][1000 genomes]
rs72699464	1.00[ASN][1000 genomes]
rs72699473	1.00[ASN][1000 genomes]
rs72699475	1.00[ASN][1000 genomes]
rs72699476	1.00[ASN][1000 genomes]
rs72699477	1.00[ASN][1000 genomes]
rs72699483	1.00[ASN][1000 genomes]
rs72699484	1.00[ASN][1000 genomes]
rs72699502	1.00[ASN][1000 genomes]
rs72701514	1.00[ASN][1000 genomes]
rs72701516	1.00[ASN][1000 genomes]
rs72701533	1.00[ASN][1000 genomes]
rs72701535	1.00[ASN][1000 genomes]
rs72701538	1.00[ASN][1000 genomes]
rs72701541	1.00[ASN][1000 genomes]
rs72701542	1.00[ASN][1000 genomes]
rs72701543	1.00[ASN][1000 genomes]
rs72701544	1.00[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	nsv1021605	chr9:18002205-18271109	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv892680	chr9:18089614-18267185	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv892681	chr9:18127068-18250459	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv892682	chr9:18166112-18272700	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv831522	chr9:18231982-18459492	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18225800-18260600	Weak transcription	Aorta	Aorta
2	chr9:18234000-18237800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr9:18234400-18237800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr9:18235200-18241000	Enhancers	Hela-S3	cervix
5	chr9:18235600-18236000	Enhancers	NHEK	skin
6	chr9:18235800-18237600	Weak transcription	HMEC	breast
7	chr9:18235800-18238000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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