Variant report

Variant	rs10816590
Chromosome Location	chr9:110700471-110700472
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10759269	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10816591	0.92[EUR][1000 genomes]
rs10816592	0.91[EUR][1000 genomes]
rs10816593	0.91[EUR][1000 genomes]
rs10816596	0.80[EUR][1000 genomes]
rs6477606	1.00[CHB][hapmap]
rs7026539	0.91[EUR][1000 genomes]
rs7041168	0.92[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	nsv893701	chr9:110650482-110709587	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 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	chr9:110694000-110701000	Weak transcription	Spleen	Spleen
2	chr9:110695800-110701200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr9:110695800-110705200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr9:110696000-110701000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr9:110696200-110707800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:110700400-110702200	Enhancers	Primary hematopoietic stem cells	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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