Variant report

Variant	rs58187497
Chromosome Location	chr11:64733838-64733839
allele	C/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:18)

rs_ID	r²[population]
rs10488702	0.84[EUR][1000 genomes]
rs17146506	0.89[EUR][1000 genomes]
rs17146508	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17146511	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17146515	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17146519	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17146528	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17146539	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17146541	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17146543	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17146544	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17146569	0.92[AMR][1000 genomes]
rs17146575	0.92[AMR][1000 genomes]
rs17673281	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4320955	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60401184	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60935617	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7482817	1.00[AMR][1000 genomes];0.89[EUR][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	nsv526181	chr11:64638041-65257329	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1539 gene(s)	inside rSNPs	diseases
2	nsv555208	chr11:64645119-64771179	Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1029 gene(s)	inside rSNPs	diseases
3	nsv976460	chr11:64727780-64743097	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 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	chr11:64728600-64736400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:64730200-64738400	Weak transcription	Stomach Mucosa	stomach

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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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