Variant report

Variant	rs66687047
Chromosome Location	chr11:74843491-74843492
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11827488	0.88[ASN][1000 genomes]
rs12281823	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12361277	0.92[ASN][1000 genomes]
rs12421194	0.81[ASN][1000 genomes]
rs17133732	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4100076	0.86[ASN][1000 genomes]
rs4944072	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4944974	0.88[ASN][1000 genomes]
rs55986601	0.88[ASN][1000 genomes]
rs58626404	0.91[ASN][1000 genomes]
rs61117837	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6592602	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67947132	0.92[ASN][1000 genomes]
rs7122309	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72996586	0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74842000-74851400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:74843400-74843600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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