Variant report

Variant	rs66747516
Chromosome Location	chr3:22393439-22393440
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11916622	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11923030	0.94[EUR][1000 genomes]
rs57865745	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66607699	0.94[EUR][1000 genomes]
rs66986313	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67095441	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs67227208	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73039270	1.00[EUR][1000 genomes]
rs73039276	1.00[EUR][1000 genomes]
rs73041314	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73041322	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73041330	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73041334	0.95[ASN][1000 genomes]
rs73041338	0.95[ASN][1000 genomes]
rs73041341	0.95[ASN][1000 genomes]
rs73041346	0.95[ASN][1000 genomes]
rs73041347	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003085	chr3:21887971-22415107	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv432404	chr3:22000296-22433396	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1003211	chr3:22244883-22584229	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv536520	chr3:22244883-22584229	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22391400-22393600	Enhancers	Fetal Lung	lung
2	chr3:22393400-22394600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr3:22393400-22394800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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