Variant report

Variant	rs12323068
Chromosome Location	chr13:93279249-93279250
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10161676	1.00[JPT][hapmap]
rs12323052	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs34547215	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4773691	0.85[ASN][1000 genomes]
rs9584044	1.00[JPT][hapmap]
rs9584045	1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs9584046	1.00[JPT][hapmap]
rs9584049	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9589591	1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs9589592	1.00[JPT][hapmap]
rs9589596	1.00[AMR][1000 genomes]
rs9589606	1.00[JPT][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456070	chr13:93208593-93298523	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv562730	chr13:93208593-93298523	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1124	chr13:93242968-93289282	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1045395	chr13:93248456-93323269	Enhancers Weak transcription	Chromatin interactive region	n/a	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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