Variant report

Variant	rs10122669
Chromosome Location	chr9:116555771-116555772
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10817521	0.86[ASN][1000 genomes]
rs10981928	0.84[EUR][1000 genomes]
rs10981930	0.86[ASN][1000 genomes]
rs12551439	0.83[ASN][1000 genomes]
rs7030473	0.99[ASN][1000 genomes]
rs7046380	0.99[ASN][1000 genomes]
rs7046526	0.99[ASN][1000 genomes]
rs7046799	0.99[ASN][1000 genomes]
rs913078	0.87[ASN][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	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116551400-116556000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr9:116552000-116555800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:116555600-116556200	Bivalent Enhancer	HepG2	liver

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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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