Variant report

Variant	rs9448511
Chromosome Location	chr6:79326092-79326093
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs16890160	1.00[EUR][1000 genomes]
rs7746614	1.00[EUR][1000 genomes]
rs9443576	1.00[EUR][1000 genomes]
rs9443585	1.00[EUR][1000 genomes]
rs9443595	1.00[EUR][1000 genomes]
rs9443596	1.00[EUR][1000 genomes]
rs9443597	1.00[EUR][1000 genomes]
rs9443598	1.00[EUR][1000 genomes]
rs9443605	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9448429	1.00[EUR][1000 genomes]
rs9448438	1.00[EUR][1000 genomes]
rs9448441	1.00[EUR][1000 genomes]
rs9448471	1.00[EUR][1000 genomes]
rs9448472	1.00[EUR][1000 genomes]
rs9448473	1.00[EUR][1000 genomes]
rs9448475	1.00[EUR][1000 genomes]
rs9448480	1.00[EUR][1000 genomes]
rs9448481	1.00[EUR][1000 genomes]
rs9448485	1.00[EUR][1000 genomes]
rs9448486	1.00[EUR][1000 genomes]
rs9448487	1.00[EUR][1000 genomes]
rs9448488	1.00[EUR][1000 genomes]
rs9448502	1.00[EUR][1000 genomes]
rs9448504	1.00[EUR][1000 genomes]
rs9448507	1.00[EUR][1000 genomes]
rs9448509	1.00[EUR][1000 genomes]
rs9448510	1.00[EUR][1000 genomes]
rs9448512	1.00[EUR][1000 genomes]
rs9448513	1.00[EUR][1000 genomes]
rs9448517	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9448533	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886235	chr6:78861808-79369972	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv604011	chr6:79042990-79455282	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv886300	chr6:79129963-79341891	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv522646	chr6:79185106-79333988	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1028767	chr6:79200713-79341224	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:79325400-79328000	Weak transcription	Ovary	ovary
2	chr6:79325600-79326800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr6:79325600-79333400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:79325800-79333400	Weak transcription	NHEK	skin
5	chr6:79326000-79328400	Weak transcription	Hela-S3	cervix

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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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