Variant report

Variant	rs7765552
Chromosome Location	chr6:147347853-147347854
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11963476	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs11966941	0.85[AFR][1000 genomes]
rs6924219	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6924244	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73586148	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73586152	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73586155	0.81[AMR][1000 genomes]
rs73586173	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs73586175	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs73586177	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7748514	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147343800-147364800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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