Variant report

Variant	rs9847565
Chromosome Location	chr3:146369166-146369167
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10513285	0.92[ASN][1000 genomes]
rs10935636	0.85[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs11717209	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs11916605	0.84[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs11924592	0.84[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs1858326	0.90[ASN][1000 genomes]
rs1858327	0.85[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2868443	0.83[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs57946797	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59201113	0.92[ASN][1000 genomes]
rs6807202	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs73159158	0.85[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs7430081	0.92[ASN][1000 genomes]
rs9842222	0.86[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	nsv516386	chr3:146366513-146758405	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv4047	chr3:146368154-146401858	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146361400-146370800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr3:146361400-146371800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:146362600-146372800	Weak transcription	Dnd41	blood
4	chr3:146368400-146369600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr3:146368600-146369600	Enhancers	Adipose Nuclei	Adipose
6	chr3:146369000-146371000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr3:146369000-146373000	Weak transcription	H9 Derived Neuronal Progenitor 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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