Variant report

Variant	rs11032462
Chromosome Location	chr11:33972549-33972550
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11032463	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11032464	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11032466	0.89[EUR][1000 genomes]
rs11602178	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11603626	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11605421	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11607752	0.87[EUR][1000 genomes]
rs12417148	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12417766	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12421417	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2421466	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35661841	0.98[EUR][1000 genomes]
rs57177321	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33965000-33974400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr11:33970800-33974200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr11:33971000-33974000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:33971200-33974000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:33972200-33973800	Weak transcription	K562	blood

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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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