Variant report

Variant	rs13052509
Chromosome Location	chr21:16143716-16143717
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12053660	0.82[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs13046559	0.86[EUR][1000 genomes]
rs13049498	0.89[EUR][1000 genomes]
rs2822923	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2822924	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs2822925	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2822928	0.96[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs35076443	0.89[EUR][1000 genomes]
rs7277958	0.86[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16143400-16146200	Enhancers	K562	blood
2	chr21:16143600-16143800	Enhancers	Thymus	Thymus
3	chr21:16143600-16144800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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