Variant report

Variant	rs73443757
Chromosome Location	chr7:126963833-126963834
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs58475352	1.00[AMR][1000 genomes]
rs58906619	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73443735	1.00[AMR][1000 genomes]
rs73443751	1.00[AMR][1000 genomes]
rs73445314	1.00[AMR][1000 genomes]
rs73445345	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73455355	1.00[AMR][1000 genomes]
rs73457180	1.00[AMR][1000 genomes]
rs73457184	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73457186	1.00[AMR][1000 genomes]
rs73457202	1.00[AMR][1000 genomes]
rs73459009	1.00[AMR][1000 genomes]
rs73459014	1.00[AMR][1000 genomes]
rs73459017	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv967497	chr7:126958676-126966982	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126963000-126964200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
2	chr7:126963200-126964000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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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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