Variant report

Variant	rs56372522
Chromosome Location	chr9:110419777-110419778
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10116391	1.00[AMR][1000 genomes]
rs10119819	1.00[AMR][1000 genomes]
rs10121640	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12337942	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12343270	1.00[EUR][1000 genomes]
rs12345789	1.00[EUR][1000 genomes]
rs12345925	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55685304	1.00[EUR][1000 genomes]
rs56772234	1.00[EUR][1000 genomes]
rs57603479	1.00[EUR][1000 genomes]
rs57608579	1.00[EUR][1000 genomes]
rs58147006	1.00[AMR][1000 genomes]
rs58221262	1.00[EUR][1000 genomes]
rs58811653	1.00[EUR][1000 genomes]
rs58884117	1.00[EUR][1000 genomes]
rs59172464	1.00[EUR][1000 genomes]
rs59870347	1.00[EUR][1000 genomes]
rs60310917	1.00[EUR][1000 genomes]
rs60510252	1.00[EUR][1000 genomes]
rs60813893	1.00[EUR][1000 genomes]
rs61080976	1.00[EUR][1000 genomes]
rs73653647	1.00[EUR][1000 genomes]
rs73653648	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831683	chr9:110275212-110461288	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv893700	chr9:110365337-110451516	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv521747	chr9:110418574-110441113	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110413000-110437000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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Input of quick search could be:

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

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