Variant report

Variant	rs13082036
Chromosome Location	chr3:68505606-68505607
allele	A/G
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:18)

rs_ID	r²[population]
rs12485360	0.96[CEU][hapmap];1.00[YRI][hapmap]
rs13072630	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs13076215	0.96[CEU][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13081659	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13087359	0.82[EUR][1000 genomes]
rs1397247	0.89[CEU][hapmap];0.86[YRI][hapmap]
rs1510348	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs1553823	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1588430	0.81[EUR][1000 genomes]
rs2221757	0.88[CEU][hapmap];0.81[YRI][hapmap];0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34778733	0.82[EUR][1000 genomes]
rs4855477	0.85[AMR][1000 genomes]
rs907082	0.82[EUR][1000 genomes]
rs9310080	0.86[JPT][hapmap];0.85[AMR][1000 genomes]
rs971231	0.83[EUR][1000 genomes]
rs9826916	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9832666	0.85[AMR][1000 genomes]
rs9990177	0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834721	chr3:68365963-68526394	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1003779	chr3:68470899-68517125	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv1832396	chr3:68478762-68641509	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv876927	chr3:68505398-68544442	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv876928	chr3:68505398-68551172	Enhancers Weak transcription ZNF genes & repeats	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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