Variant report

Variant	rs58897658
Chromosome Location	chr4:166474634-166474635
allele	G/T
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]
rs17046582	1.00[AMR][1000 genomes]
rs17046625	1.00[AMR][1000 genomes]
rs17046632	1.00[AMR][1000 genomes]
rs58493479	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59397196	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61073284	1.00[AMR][1000 genomes]
rs61552650	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72976184	1.00[AMR][1000 genomes]
rs72976187	1.00[AMR][1000 genomes]
rs7660700	1.00[AMR][1000 genomes]
rs9683908	0.92[AFR][1000 genomes];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	nsv508327	chr4:166424440-166475679	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv596052	chr4:166454826-166488615	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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