Variant report

Variant	rs16840218
Chromosome Location	chr3:133034858-133034859
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10428212	0.84[AFR][1000 genomes]
rs16840130	0.84[AFR][1000 genomes]
rs16840157	0.84[AFR][1000 genomes]
rs4292227	0.84[AFR][1000 genomes]
rs57407869	0.84[AFR][1000 genomes]
rs58668505	0.84[AFR][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	nsv1014344	chr3:133024614-133042938	Enhancers ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133016400-133038200	Weak transcription	Fetal Lung	lung
2	chr3:133021000-133037600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:133034000-133038000	Enhancers	Fetal Brain Male	brain
4	chr3:133034400-133036600	Enhancers	Fetal Brain Female	brain

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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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