Variant report

Variant	rs60004284
Chromosome Location	chr10:93124038-93124039
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs56086306	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56182786	1.00[AMR][1000 genomes]
rs56781866	1.00[AMR][1000 genomes]
rs59669716	1.00[AMR][1000 genomes]
rs61658197	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150656	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150657	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150659	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150660	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150661	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150663	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150664	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150665	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150666	0.87[AFR][1000 genomes];1.00[AMR][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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