Variant report

Variant	rs10136169
Chromosome Location	chr14:42484127-42484128
allele	A/G
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:7)

rs_ID	r²[population]
rs10147564	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10150078	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28605682	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28616607	0.97[ASN][1000 genomes]
rs34813012	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8013328	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8013800	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv564563	chr14:42477256-42644617	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42480000-42484200	Enhancers	Primary B cells from cord blood	blood
2	chr14:42484000-42484400	Enhancers	Primary B cells from peripheral blood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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