Variant report

Variant	rs58028555
Chromosome Location	chr8:51594893-51594894
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs55891616	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56404315	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56411134	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60368645	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60417957	1.00[AMR][1000 genomes]
rs73676385	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73676390	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73677532	1.00[AMR][1000 genomes]
rs73678629	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73678631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73678691	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948436	chr8:51115028-51917504	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv429914	chr8:51371447-51617647	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv531502	chr8:51390997-51703556	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3514165	chr8:51416583-51923545	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv3514166	chr8:51416583-51923545	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv890873	chr8:51462163-51612641	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv1027452	chr8:51525439-51725489	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51570200-51595200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:51592000-51596000	Weak transcription	Brain Germinal Matrix	brain
3	chr8:51594400-51596200	Enhancers	Liver	Liver
4	chr8:51594600-51595200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr8:51594600-51596400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr8:51594800-51595200	Weak transcription	NH-A	brain

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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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