Variant report

Variant	rs73550944
Chromosome Location	chr9:116551847-116551848
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs60769152	1.00[AMR][1000 genomes]
rs73548477	1.00[AMR][1000 genomes]
rs73548538	1.00[AMR][1000 genomes]
rs73548540	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73548554	1.00[AMR][1000 genomes]
rs73548557	1.00[AMR][1000 genomes]
rs73550446	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73550942	1.00[AMR][1000 genomes]
rs73550967	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73552319	1.00[AMR][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	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116550000-116553800	Enhancers	Brain Germinal Matrix	brain
2	chr9:116550600-116552400	Bivalent Enhancer	Fetal Brain Male	brain
3	chr9:116551400-116552000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:116551400-116556000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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

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