Variant report

Variant	rs34073861
Chromosome Location	chr11:33979297-33979298
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1518919	1.00[AMR][1000 genomes]
rs1546671	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1589183	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2056250	1.00[AMR][1000 genomes]
rs2901433	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34166865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35565294	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35743871	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35755947	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4429033	1.00[AMR][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33976600-33981400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr11:33977200-33981200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr11:33977800-33979400	Enhancers	HUVEC	blood vessel
4	chr11:33978000-33981400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr11:33978400-33979400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr11:33978400-33980000	Enhancers	K562	blood
7	chr11:33979200-33981400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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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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