Variant report

Variant	rs12417766
Chromosome Location	chr11:33978959-33978960
allele	A/G
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[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11603626	1.00[AMR][1000 genomes];1.00[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]
rs12421417	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2421466	1.00[AFR][1000 genomes];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	chr11:33976600-33981400	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	chr11:33978600-33979200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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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