Variant report

Variant	rs13289287
Chromosome Location	chr9:73503774-73503775
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12000979	0.81[ASN][1000 genomes]
rs13283806	0.86[ASN][1000 genomes]
rs13287493	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13290594	0.83[ASN][1000 genomes]
rs13293998	0.82[CHB][hapmap];0.86[CHD][hapmap];0.83[ASN][1000 genomes]
rs1337010	0.82[CHB][hapmap];0.86[CHD][hapmap];0.81[ASN][1000 genomes]
rs1361028	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4143736	0.82[EUR][1000 genomes]
rs9792446	0.81[ASN][1000 genomes]
rs9792690	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893441	chr9:73486034-73594114	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv818705	chr9:73500857-73510880	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv3483093	chr9:73500939-73514808	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
4	esv3483094	chr9:73500939-73514808	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	nsv442152	chr9:73502255-73507221	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3693031	chr9:73502424-73510880	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	nsv818706	chr9:73502424-73510880	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	nsv516833	chr9:73502424-73514958	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73503600-73503800	Enhancers	HUVEC	blood vessel

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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