Variant report

Variant	rs10034043
Chromosome Location	chr4:147818113-147818114
allele	G/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]
rs1396718	0.80[AMR][1000 genomes]
rs1437263	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1469921	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1509333	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2028126	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2289164	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2304536	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28676537	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62329363	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs748826	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs748827	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs881591	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs882189	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs969510	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147817800-147820800	Weak transcription	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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