Variant report

Variant	rs73584758
Chromosome Location	chr8:50819829-50819830
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10113044	1.00[AMR][1000 genomes]
rs16913838	1.00[AMR][1000 genomes]
rs16913859	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16913881	1.00[AMR][1000 genomes]
rs16913981	1.00[AMR][1000 genomes]
rs16914042	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16914070	1.00[AMR][1000 genomes]
rs2306742	1.00[AMR][1000 genomes]
rs28529396	1.00[AMR][1000 genomes]
rs57307349	1.00[AMR][1000 genomes]
rs57882761	1.00[AMR][1000 genomes]
rs58254228	1.00[AMR][1000 genomes]
rs58520473	1.00[AMR][1000 genomes]
rs60153766	1.00[AMR][1000 genomes]
rs60356093	1.00[AMR][1000 genomes]
rs61374770	1.00[AMR][1000 genomes]
rs73569305	1.00[AMR][1000 genomes]
rs73569306	1.00[AMR][1000 genomes]
rs73569315	1.00[AMR][1000 genomes]
rs73569317	1.00[AMR][1000 genomes]
rs73569327	1.00[AMR][1000 genomes]
rs73569333	1.00[AMR][1000 genomes]
rs73569338	1.00[AMR][1000 genomes]
rs73569339	1.00[AMR][1000 genomes]
rs73569343	1.00[AMR][1000 genomes]
rs73584719	1.00[AMR][1000 genomes]
rs73584722	1.00[AMR][1000 genomes]
rs73584723	1.00[AMR][1000 genomes]
rs73584728	1.00[AMR][1000 genomes]
rs73584754	1.00[AMR][1000 genomes]
rs73584759	1.00[AMR][1000 genomes]
rs73584763	1.00[AMR][1000 genomes]
rs73584765	1.00[AMR][1000 genomes]
rs73584768	1.00[AMR][1000 genomes]
rs73584770	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73584771	1.00[AMR][1000 genomes]
rs73584773	1.00[AMR][1000 genomes]
rs73676082	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	esv3353749	chr8:50530807-51139242	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:50816000-50821800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:50818400-50821400	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr8:50819600-50820200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:50819800-50820000	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr8:50819800-50820400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	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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