Variant report

Variant	rs11700673
Chromosome Location	chr21:40064571-40064572
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11088437	0.91[EUR][1000 genomes]
rs2212606	0.81[EUR][1000 genomes]
rs2836615	0.83[EUR][1000 genomes]
rs2836621	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2836631	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2836633	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2836634	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2836635	0.93[EUR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40040000-40071200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr21:40060000-40073200	Weak transcription	Aorta	Aorta
3	chr21:40063400-40065200	Enhancers	HUVEC	blood vessel
4	chr21:40063600-40067400	Weak transcription	Ovary	ovary
5	chr21:40064000-40065600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr21:40064000-40065600	Enhancers	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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