Variant report

Variant	rs28520988
Chromosome Location	chr18:28705511-28705512
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs16948612	1.00[AMR][1000 genomes]
rs2043734	1.00[AMR][1000 genomes]
rs28584973	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28620831	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7240259	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9946137	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9957402	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9957506	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9961861	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9963657	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9964449	1.00[AMR][1000 genomes]

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	nsv530788	chr18:28596461-28751891	Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	esv3360998	chr18:28693111-28881812	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr18:28703200-28708200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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