Variant report

Variant	rs2768639
Chromosome Location	chr9:96967460-96967461
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1310978	0.85[AMR][1000 genomes]
rs17350072	0.94[EUR][1000 genomes]
rs1769261	0.85[AMR][1000 genomes]
rs2094525	0.85[AMR][1000 genomes]
rs2790413	0.85[AMR][1000 genomes]
rs2987202	0.85[AMR][1000 genomes]
rs3118763	0.85[AMR][1000 genomes]
rs3118767	0.85[AMR][1000 genomes]
rs4578010	0.85[AMR][1000 genomes]
rs608328	0.85[AMR][1000 genomes]
rs6479532	0.85[AMR][1000 genomes]
rs7045634	0.85[AMR][1000 genomes]
rs7867660	0.85[AMR][1000 genomes]
rs9409761	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482457	chr9:96813852-96996170	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	217 gene(s)	inside rSNPs	diseases
2	nsv831655	chr9:96834042-97042009	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	218 gene(s)	inside rSNPs	diseases
3	esv3394266	chr9:96935210-97045514	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	195 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96961200-96973600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr9:96963000-96970200	Weak transcription	Gastric	stomach
3	chr9:96963200-96971200	Weak transcription	Aorta	Aorta

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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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