Variant report

Variant	rs9487029
Chromosome Location	chr6:109596115-109596116
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1008083	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs1608043	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55863350	0.92[AFR][1000 genomes]
rs61002917	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6568562	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6568565	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6909900	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6924768	0.85[AFR][1000 genomes]
rs73512467	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs73518692	0.90[AFR][1000 genomes]
rs73520752	0.81[AFR][1000 genomes]
rs73520760	0.81[AFR][1000 genomes]
rs73762681	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7743328	0.81[AFR][1000 genomes]
rs7753882	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7754671	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7762891	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7773100	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9480917	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9480925	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9487018	0.84[AFR][1000 genomes]
rs9487030	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9487035	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9487044	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9487045	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9487050	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9487056	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9487059	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs949883	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109587600-109614600	Weak transcription	HepG2	liver
2	chr6:109591600-109615200	Weak transcription	Placenta	Placenta

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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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