Variant report

Variant	rs28375440
Chromosome Location	chr4:166716686-166716687
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10030523	1.00[AMR][1000 genomes]
rs10050131	1.00[AMR][1000 genomes]
rs28583095	1.00[AMR][1000 genomes]
rs28602324	1.00[AMR][1000 genomes]
rs28607794	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28633958	1.00[AMR][1000 genomes]
rs28816187	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28830841	1.00[AMR][1000 genomes]
rs72980044	1.00[AMR][1000 genomes]
rs72980072	1.00[AMR][1000 genomes]
rs72982290	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7356239	1.00[AMR][1000 genomes]
rs73863245	1.00[AMR][1000 genomes]
rs9308119	1.00[AMR][1000 genomes]
rs9985659	1.00[AMR][1000 genomes]
rs9985705	1.00[AMR][1000 genomes]
rs9995426	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754222	chr4:166606890-166737921	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv3490569	chr4:166680129-166981346	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv3490570	chr4:166680129-166981346	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr4:166709000-166719600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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