Variant report

Variant	rs813755
Chromosome Location	chr8:64538578-64538579
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs1149458	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1149459	0.88[AFR][1000 genomes];0.80[EUR][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:5 , 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	chr8:64537400-64539000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:64537400-64539200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr8:64537800-64538800	Weak transcription	HMEC	breast
5	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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