Variant report

Variant	rs73108632
Chromosome Location	chr5:59675274-59675275
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs57558762	1.00[AMR][1000 genomes]
rs59813460	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60452961	1.00[AMR][1000 genomes]
rs61245506	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6895769	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73104768	1.00[AMR][1000 genomes]
rs73106733	1.00[AMR][1000 genomes]
rs73106783	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73108651	1.00[AMR][1000 genomes]
rs73108656	1.00[AMR][1000 genomes]
rs7706015	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	nsv1025856	chr5:59188419-59928852	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv830316	chr5:59480269-59689829	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv598288	chr5:59627555-60003460	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59647200-59694200	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59662600-59680200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr5:59674800-59675800	Enhancers	Aorta	Aorta
4	chr5:59674800-59675800	Enhancers	GM12878-XiMat	blood

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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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