Variant report

Variant	rs58092050
Chromosome Location	chr10:93123962-93123963
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs56996606	1.00[EUR][1000 genomes]
rs58377848	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60608782	1.00[EUR][1000 genomes]
rs60829821	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61386275	0.91[AMR][1000 genomes]
rs74150650	1.00[EUR][1000 genomes]
rs74150658	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150662	1.00[EUR][1000 genomes]
rs7908999	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7909381	1.00[EUR][1000 genomes]
rs7909527	1.00[EUR][1000 genomes]
rs7919744	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93113800-93136600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:93121000-93126200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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