Variant report

Variant	rs2421466
Chromosome Location	chr11:33985242-33985243
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];0.93[EUR][1000 genomes]
rs11032463	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11032464	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11032466	0.96[EUR][1000 genomes]
rs11602178	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11603626	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11605421	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11607752	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12417148	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12417766	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12421417	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35661841	0.91[EUR][1000 genomes]
rs57177321	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33981400-33985600	Enhancers	K562	blood
2	chr11:33983200-33992400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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