Variant report

Variant	rs6914147
Chromosome Location	chr6:75753175-75753176
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]
rs10455309	0.88[EUR][1000 genomes]
rs12055814	0.95[EUR][1000 genomes]
rs12173437	0.81[EUR][1000 genomes]
rs1412275	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4432952	0.81[EUR][1000 genomes]
rs6453808	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6453812	0.92[EUR][1000 genomes]
rs6916346	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73745751	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs765796	0.90[EUR][1000 genomes]
rs7771969	0.92[EUR][1000 genomes]
rs9343266	0.92[EUR][1000 genomes]
rs9352181	0.97[EUR][1000 genomes]
rs9359116	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75750400-75753200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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