Variant report

Variant	rs16969362
Chromosome Location	chr15:33617186-33617187
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs16969003	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs16969320	1.00[CHB][hapmap];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16969324	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2339266	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3817326	1.00[GIH][hapmap]
rs4271563	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5027490	0.91[ASN][1000 genomes]
rs57740853	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73374800	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73378425	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73378430	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8027734	0.85[ASN][1000 genomes]
rs8039430	0.89[ASN][1000 genomes]
rs907954	1.00[CHB][hapmap];0.97[EUR][1000 genomes];0.89[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	nsv482299	chr15:33449137-33624122	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv533346	chr15:33469439-33809641	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv832963	chr15:33514798-33712442	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv832964	chr15:33608771-33784018	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33615600-33617200	Enhancers	Primary B cells from peripheral blood	blood
2	chr15:33616200-33620400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr15:33616200-33620800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr15:33616400-33617400	Weak transcription	Thymus	Thymus

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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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