Variant report

Variant	rs7001039
Chromosome Location	chr8:129836915-129836916
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1879162	1.00[EUR][1000 genomes]
rs2090682	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35208579	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3857887	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4733651	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4733660	0.82[EUR][1000 genomes]
rs6470664	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6994324	0.96[EUR][1000 genomes]
rs7463635	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs919658	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129836200-129837200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:129836400-129837000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:129836400-129837000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:129836400-129837200	Enhancers	K562	blood
5	chr8:129836600-129837200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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