Variant report

Variant	rs73269072
Chromosome Location	chr8:64537957-64537958
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs6994952	1.00[AMR][1000 genomes]
rs73269080	1.00[AMR][1000 genomes]
rs73270941	1.00[AMR][1000 genomes]
rs73270950	1.00[AMR][1000 genomes]
rs73270961	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	nsv831343	chr8:64436268-64642328	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64535400-64540400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:64537400-64538400	Enhancers	NHEK	skin
3	chr8:64537400-64539000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr8:64537400-64539200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr8:64537800-64538800	Weak transcription	HMEC	breast
6	chr8:64537800-64538800	Weak transcription	NH-A	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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