Variant report

Variant	rs4708028
Chromosome Location	chr6:73806566-73806567
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1113015	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1113016	0.81[AMR][1000 genomes]
rs11965567	0.81[AMR][1000 genomes]
rs1418414	0.81[AMR][1000 genomes]
rs4235873	0.92[AMR][1000 genomes]
rs4706528	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4708033	0.91[AMR][1000 genomes]
rs6904597	0.81[AMR][1000 genomes]
rs6911409	0.88[AMR][1000 genomes]
rs6927120	0.81[AMR][1000 genomes]
rs6927134	0.91[AMR][1000 genomes]
rs6927759	0.89[AMR][1000 genomes]
rs6927779	0.95[AMR][1000 genomes]
rs6933361	0.91[AMR][1000 genomes]
rs73452859	0.81[AMR][1000 genomes]
rs73452861	0.81[AMR][1000 genomes]
rs7743399	0.81[AMR][1000 genomes]
rs7764571	0.83[AMR][1000 genomes]
rs7772526	0.86[AMR][1000 genomes]
rs7776435	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9293920	0.92[AMR][1000 genomes]
rs9341404	0.91[AMR][1000 genomes]
rs9341408	0.91[AMR][1000 genomes]
rs9341409	0.91[AMR][1000 genomes]
rs9343006	0.92[AMR][1000 genomes]
rs9343009	0.88[AMR][1000 genomes]
rs9350488	0.91[AMR][1000 genomes]
rs9350489	0.91[AMR][1000 genomes]
rs9360636	0.92[AMR][1000 genomes]
rs9360640	0.86[AMR][1000 genomes]
rs9442887	0.91[AMR][1000 genomes]
rs9446844	0.88[AMR][1000 genomes]
rs9446845	0.86[AMR][1000 genomes]
rs9446851	0.83[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3410973	chr6:73716033-74419545	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 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	chr6:73791000-73830600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:73805200-73806600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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