Variant report

Variant	rs57370598
Chromosome Location	chr5:15966899-15966900
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10037441	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10042891	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10064082	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1604475	1.00[ASN][1000 genomes]
rs16867862	1.00[ASN][1000 genomes]
rs1868960	1.00[ASN][1000 genomes]
rs1961472	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28669234	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56304070	1.00[ASN][1000 genomes]
rs56800685	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59324866	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6867247	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73753910	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv830216	chr5:15860662-16060420	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv427712	chr5:15883439-16055856	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA	4 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	chr5:15966200-15967000	Enhancers	Fetal Heart	heart
2	chr5:15966400-15967000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:15966400-15967200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:15966400-15967200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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