Variant report

Variant	rs57332857
Chromosome Location	chr13:97678442-97678443
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1501862	0.83[AMR][1000 genomes]
rs7328024	0.85[AMR][1000 genomes]
rs73550844	0.85[AMR][1000 genomes]
rs74107003	0.83[AMR][1000 genomes]
rs74107008	0.83[AMR][1000 genomes]
rs74107009	0.83[AMR][1000 genomes]
rs74107011	0.83[AMR][1000 genomes]
rs7983514	0.85[AMR][1000 genomes]
rs7986614	0.85[AMR][1000 genomes]
rs7987624	0.85[AMR][1000 genomes]
rs7992251	1.00[AMR][1000 genomes]
rs9300383	0.85[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	nsv832693	chr13:97594845-97777481	Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:97676600-97679000	Weak transcription	Hela-S3	cervix
2	chr13:97678000-97678800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr13:97678200-97679000	Enhancers	Adipose Nuclei	Adipose
4	chr13:97678400-97678800	Weak transcription	Fetal Brain Male	brain
5	chr13:97678400-97679000	Enhancers	HUVEC	blood vessel

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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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