Variant report

Variant	rs10110699
Chromosome Location	chr8:64511275-64511276
allele	C/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]
rs13265819	0.81[EUR][1000 genomes]
rs2084862	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	chr8:64505000-64514400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:64509800-64516000	Weak transcription	Brain Germinal Matrix	brain
3	chr8:64510200-64515000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr8:64510600-64513200	Weak transcription	Fetal Brain Male	brain
5	chr8:64510800-64512000	Enhancers	Monocytes-CD14+_RO01746	blood

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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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