Variant report

Variant	rs4738640
Chromosome Location	chr8:58805473-58805474
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10095403	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11786413	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13250052	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13253940	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs13256902	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13273087	0.90[ASN][1000 genomes]
rs13274347	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1865724	0.90[ASN][1000 genomes]
rs2082911	0.87[ASN][1000 genomes]
rs34390402	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs35132214	0.94[ASN][1000 genomes]
rs35769297	0.90[ASN][1000 genomes]
rs35939921	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4145789	0.88[ASN][1000 genomes]
rs4738634	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4738638	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831323	chr8:58692548-58849862	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No data

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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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