Variant report

Variant	rs73566767
Chromosome Location	chr8:34374498-34374499
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs2609615	1.00[AMR][1000 genomes]
rs60827370	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73566761	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73566766	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73568367	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73568371	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73568376	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73568393	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73568394	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73568395	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73568396	0.93[AFR][1000 genomes]
rs73577336	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73579476	0.82[AFR][1000 genomes];1.00[AMR][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	esv1847298	chr8:34356954-34376347	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
2	esv3428603	chr8:34367445-34422532	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34372800-34379200	Weak transcription	Fetal Heart	heart
2	chr8:34374000-34374800	Enhancers	Brain Germinal Matrix	brain

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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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