Variant report

Variant	rs3812530
Chromosome Location	chr9:73485048-73485049
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11142635	0.95[ASN][1000 genomes]
rs12000979	0.83[ASN][1000 genomes]
rs13290594	0.81[ASN][1000 genomes]
rs13293998	0.95[CEU][hapmap];0.90[CHB][hapmap];1.00[GIH][hapmap];0.81[JPT][hapmap];0.92[TSI][hapmap];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1337010	0.90[CHB][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs9792446	0.83[ASN][1000 genomes]
rs9792690	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73457200-73485200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:73484200-73488200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:73484200-73488200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:73484200-73488200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr9:73484200-73488400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:73484400-73487600	Weak transcription	Muscle Satellite Cultured Cells	--

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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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