Variant report

Variant	rs9663396
Chromosome Location	chr10:45596024-45596025
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11239349	0.82[ASN][1000 genomes]
rs12252994	0.90[ASN][1000 genomes]
rs12569983	0.89[ASN][1000 genomes]
rs12570593	0.90[ASN][1000 genomes]
rs28510585	0.82[ASN][1000 genomes]
rs55648726	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60197913	0.95[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73291619	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7907860	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831848	chr10:45490176-45667670	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
2	esv2750897	chr10:45550145-45820136	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 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	chr10:45590400-45596400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:45591000-45602000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr10:45595600-45596200	Enhancers	Brain Germinal Matrix	brain
4	chr10:45596000-45596600	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr10:45596000-45596600	Bivalent Enhancer	Brain Hippocampus Middle	brain
6	chr10:45596000-45596800	Enhancers	Fetal Muscle Leg	muscle

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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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