Variant report

Variant	rs6783490
Chromosome Location	chr3:156584917-156584918
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	0.93[YRI][hapmap]
rs28719920	0.80[AFR][1000 genomes]
rs28881287	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4474996	0.93[YRI][hapmap];0.86[AFR][1000 genomes]
rs58895069	1.00[AMR][1000 genomes]
rs6441097	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6441098	0.93[YRI][hapmap];0.86[AFR][1000 genomes]
rs6807765	0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs73873737	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7638335	1.00[YRI][hapmap];0.98[AFR][1000 genomes]
rs9289974	0.87[YRI][hapmap]
rs9809108	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9814973	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9820893	0.88[AFR][1000 genomes]
rs9831523	0.91[YRI][hapmap]
rs9836414	0.93[YRI][hapmap];1.00[AMR][1000 genomes]
rs9850381	0.93[YRI][hapmap];0.80[AFR][1000 genomes]
rs9862136	1.00[AMR][1000 genomes]
rs9865537	0.94[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	nsv877685	chr3:156444383-156611676	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
2	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:156581200-156585600	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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