Variant report

Variant	rs7021511
Chromosome Location	chr9:110645508-110645509
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:6)

rs_ID	r²[population]
rs10119909	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11788981	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11789958	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11793998	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13289749	0.82[EUR][1000 genomes]
rs34445584	0.83[AMR][1000 genomes];0.97[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	nsv1051101	chr9:110548257-110697253	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110635800-110656800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:110643400-110646000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr9:110644000-110645600	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr9:110644400-110647000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr9:110644400-110651000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:110644800-110658800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:110645400-110645800	Enhancers	GM12878-XiMat	blood
8	chr9:110645400-110646800	Enhancers	Primary B cells from cord blood	blood
9	chr9:110645400-110646800	Enhancers	Primary B cells from peripheral blood	blood

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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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