Variant report

Variant	rs56284969
Chromosome Location	chr5:94438069-94438070
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10515221	0.81[EUR][1000 genomes]
rs55698765	0.81[EUR][1000 genomes]
rs56005052	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56180405	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56388311	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72779413	0.82[EUR][1000 genomes]
rs72779415	0.82[EUR][1000 genomes]
rs72779419	0.82[EUR][1000 genomes]
rs72779421	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72779422	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72779432	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72779439	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72779444	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94436400-94438200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:94436400-94438600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr5:94437200-94438200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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