Variant report

Variant	rs9516076
Chromosome Location	chr13:93068719-93068720
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1023012	0.81[CEU][hapmap];0.82[MEX][hapmap];0.80[TSI][hapmap];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12877337	0.92[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1536620	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17434593	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2209834	0.86[AMR][1000 genomes]
rs2225157	0.85[AMR][1000 genomes]
rs7317334	0.86[AMR][1000 genomes]
rs7334105	0.85[AMR][1000 genomes]
rs7336824	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7985054	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8000039	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9516073	0.90[ASW][hapmap];0.83[CEU][hapmap];0.92[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.93[MEX][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9523661	0.80[TSI][hapmap]
rs9523668	0.81[CEU][hapmap]
rs9523669	0.81[CEU][hapmap]
rs9523670	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs9523671	1.00[CHB][hapmap];1.00[JPT][hapmap]

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	esv2756005	chr13:92584199-93080799	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv832680	chr13:93021114-93181489	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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