Variant report

Variant	rs11733118
Chromosome Location	chr4:79885235-79885236
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11721889	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11722107	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11723402	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11726962	0.91[EUR][1000 genomes]
rs11734417	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11735466	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1480732	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17003536	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17003542	0.92[EUR][1000 genomes]
rs17003548	0.92[EUR][1000 genomes]
rs17003571	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34390209	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56805198	0.85[EUR][1000 genomes]
rs72864015	0.92[EUR][1000 genomes]
rs72864075	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829979	chr4:79819168-80019159	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1000907	chr4:79838948-80224764	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79883400-79892800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr4:79884600-79885400	Enhancers	Aorta	Aorta
3	chr4:79885200-79885400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

Quick Search:

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

what's new

Quick links