Variant report

Variant	rs11603626
Chromosome Location	chr11:33978197-33978198
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]
rs11032462	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11032463	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11032464	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11032466	0.94[EUR][1000 genomes]
rs11602178	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11605421	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11607752	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12417148	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12417766	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12421417	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2421466	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35661841	0.93[EUR][1000 genomes]
rs57177321	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33975200-33978400	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr11:33975200-33978600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:33976600-33981400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr11:33977000-33978400	Weak transcription	K562	blood
5	chr11:33977200-33981200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:33977800-33979400	Enhancers	HUVEC	blood vessel
7	chr11:33978000-33981400	Weak transcription	Primary neutrophils fromperipheralblood	blood

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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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