Variant report

Variant	rs10264705
Chromosome Location	chr7:117596604-117596605
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10225268	1.00[AMR][1000 genomes]
rs10237349	1.00[AMR][1000 genomes]
rs10242446	1.00[AMR][1000 genomes]
rs10243584	1.00[AMR][1000 genomes]
rs10252551	1.00[AMR][1000 genomes]
rs10252658	1.00[AMR][1000 genomes]
rs10255263	1.00[AMR][1000 genomes]
rs10272355	1.00[AMR][1000 genomes]
rs28515486	1.00[AMR][1000 genomes]
rs28671130	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34033353	1.00[AMR][1000 genomes]
rs34191399	1.00[AMR][1000 genomes]
rs34232878	1.00[AMR][1000 genomes]
rs34611640	1.00[AMR][1000 genomes]
rs34693983	1.00[AMR][1000 genomes]
rs34792764	1.00[AMR][1000 genomes]
rs35631203	1.00[AMR][1000 genomes]
rs35659137	1.00[AMR][1000 genomes]
rs35743017	1.00[AMR][1000 genomes]
rs35857603	1.00[AMR][1000 genomes]
rs36089175	1.00[AMR][1000 genomes]
rs6976826	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	nsv869971	chr7:117420583-118274149	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 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	chr7:117587000-117601000	Weak transcription	Fetal Lung	lung
2	chr7:117596400-117598600	Weak transcription	Fetal Kidney	kidney

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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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