Variant report

Variant	rs9836414
Chromosome Location	chr3:156633049-156633050
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs13314352	0.90[ASW][hapmap];0.85[LWK][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs28881287	1.00[AMR][1000 genomes]
rs4474996	0.90[ASW][hapmap];0.91[MKK][hapmap];0.86[YRI][hapmap]
rs58895069	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59980662	0.90[AFR][1000 genomes]
rs6441097	0.90[ASW][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.93[YRI][hapmap];1.00[AMR][1000 genomes]
rs6441098	0.86[YRI][hapmap]
rs6783490	0.93[YRI][hapmap];1.00[AMR][1000 genomes]
rs6798879	0.84[YRI][hapmap]
rs6807765	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73873737	1.00[AMR][1000 genomes]
rs7638335	0.93[YRI][hapmap]
rs9289974	0.93[YRI][hapmap]
rs9809108	0.93[YRI][hapmap];1.00[AMR][1000 genomes]
rs9814973	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9831523	1.00[YRI][hapmap]
rs9850381	0.86[YRI][hapmap]
rs9862136	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9865537	1.00[YRI][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	nsv829765	chr3:156568263-156718496	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv592120	chr3:156626091-156691604	Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:156628600-156636600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr3:156628600-156636600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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