Variant report

Variant	rs10209798
Chromosome Location	chr2:169752951-169752952
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10179587	1.00[AMR][1000 genomes]
rs10194071	1.00[AMR][1000 genomes]
rs13384539	1.00[MEX][hapmap]
rs13414278	1.00[AMR][1000 genomes]
rs13431683	1.00[ASW][hapmap]
rs16856043	1.00[MEX][hapmap]
rs2293130	1.00[MEX][hapmap]
rs55892097	1.00[AMR][1000 genomes]
rs6715133	1.00[ASW][hapmap]
rs73969989	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	nsv583599	chr2:169664227-169903096	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 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	chr2:169747000-169757600	Weak transcription	Pancreas	Pancrea
2	chr2:169747600-169753200	Weak transcription	K562	blood
3	chr2:169751600-169753600	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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