Variant report

Variant	rs9473741
Chromosome Location	chr6:50057006-50057007
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13437462	1.00[YRI][hapmap]
rs9463564	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9463565	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9463568	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9463571	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473715	1.00[AMR][1000 genomes]
rs9473717	1.00[AMR][1000 genomes]
rs9473719	1.00[YRI][hapmap]
rs9473720	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473721	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473724	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473734	1.00[YRI][hapmap]
rs9473742	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9885929	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:50055600-50059200	Weak transcription	NHEK	skin
2	chr6:50055800-50058800	Weak transcription	HMEC	breast
3	chr6:50056200-50059000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr6:50056200-50059200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:50056600-50059000	Weak transcription	HSMM	muscle
6	chr6:50056600-50061000	Enhancers	Fetal Intestine Large	intestine

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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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