Variant report

Variant	rs6764921
Chromosome Location	chr3:179750410-179750411
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs6800787	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6806249	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73059383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73059392	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7635439	1.00[EUR][1000 genomes]
rs7648641	1.00[EUR][1000 genomes]
rs7648838	1.00[EUR][1000 genomes]
rs9816040	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9853361	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9854231	0.91[AFR][1000 genomes];1.00[EUR][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	nsv829808	chr3:179574614-179754321	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv534210	chr3:179666123-179899347	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1000756	chr3:179672703-179827373	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179726000-179754200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:179742600-179753600	Weak transcription	Pancreas	Pancrea
3	chr3:179749400-179752000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr3:179749800-179750800	Enhancers	H1 Cell Line	embryonic stem cell
5	chr3:179750000-179753000	Flanking Active TSS	Dnd41	blood
6	chr3:179750200-179750600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr3:179750400-179753400	Weak transcription	H9 Cell Line	embryonic stem cell

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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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