Variant report

Variant	rs9739059
Chromosome Location	chr12:62412424-62412425
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10506434	0.90[ASN][1000 genomes]
rs11174271	0.81[ASN][1000 genomes]
rs1121705	0.84[ASN][1000 genomes]
rs11832494	0.80[ASN][1000 genomes]
rs11835202	0.88[ASN][1000 genomes]
rs11836443	0.94[ASN][1000 genomes]
rs11836487	1.00[ASN][1000 genomes]
rs12831463	1.00[ASN][1000 genomes]
rs1373454	1.00[ASN][1000 genomes]
rs1440723	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1440724	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17125609	0.84[ASN][1000 genomes]
rs17125631	0.84[ASN][1000 genomes]
rs17654373	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17705406	1.00[ASN][1000 genomes]
rs34008431	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs56085119	0.90[ASN][1000 genomes]
rs56279780	1.00[ASN][1000 genomes]
rs7314952	0.84[ASN][1000 genomes]
rs73314023	0.90[ASN][1000 genomes]
rs9668399	1.00[ASN][1000 genomes]
rs9668407	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9668420	1.00[ASN][1000 genomes]
rs9668428	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9669003	1.00[ASN][1000 genomes]
rs9669020	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9669351	1.00[ASN][1000 genomes]
rs9669481	0.97[ASN][1000 genomes]
rs9669783	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9669794	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9739051	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039741	chr12:62046850-62491052	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv832435	chr12:62407000-62601835	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62411800-62418200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr12:62412000-62420000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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