Variant report

Variant	rs9815486
Chromosome Location	chr3:60787954-60787955
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10510854	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs12330455	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1447924	1.00[MEX][hapmap]
rs17063926	1.00[MEX][hapmap]
rs17064007	1.00[MEX][hapmap]
rs28755000	1.00[AMR][1000 genomes]
rs6762099	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9827254	1.00[MEX][hapmap]
rs9862895	1.00[MEX][hapmap]

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	nsv529602	chr3:60088353-60830769	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv998815	chr3:60495872-60830769	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv534038	chr3:60781917-60993082	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2757872	chr3:60781943-61019003	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2759152	chr3:60781943-61220809	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60786800-60789200	Enhancers	Brain Germinal Matrix	brain
2	chr3:60787000-60789200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr3:60787000-60789200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr3:60787200-60789200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:60787400-60788000	Enhancers	Fetal Lung	lung
6	chr3:60787800-60789200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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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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