Variant report

Variant	rs73076937
Chromosome Location	chr3:55808627-55808628
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs3907611	1.00[ASN][1000 genomes]
rs56163631	1.00[ASN][1000 genomes]
rs56378219	1.00[ASN][1000 genomes]
rs73075350	1.00[ASN][1000 genomes]
rs73075372	1.00[ASN][1000 genomes]
rs73076953	1.00[ASN][1000 genomes]
rs73076956	1.00[ASN][1000 genomes]
rs73078766	1.00[ASN][1000 genomes]
rs73078777	1.00[ASN][1000 genomes]
rs73083342	1.00[ASN][1000 genomes]
rs73083347	1.00[ASN][1000 genomes]
rs73083357	1.00[ASN][1000 genomes]
rs73083359	1.00[ASN][1000 genomes]
rs73083368	1.00[ASN][1000 genomes]
rs73083374	1.00[ASN][1000 genomes]
rs73083379	1.00[ASN][1000 genomes]
rs73083381	1.00[ASN][1000 genomes]
rs73086157	1.00[ASN][1000 genomes]
rs73086168	1.00[ASN][1000 genomes]
rs73086178	1.00[ASN][1000 genomes]
rs73086185	1.00[ASN][1000 genomes]
rs73086190	1.00[ASN][1000 genomes]
rs73086191	1.00[ASN][1000 genomes]
rs73086196	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	nsv876814	chr3:55802749-55860526	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:55807400-55809800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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