Variant report

Variant	rs9961262
Chromosome Location	chr18:44975549-44975550
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12968905	0.92[ASN][1000 genomes]
rs16953140	0.87[ASN][1000 genomes]
rs2004310	0.82[ASN][1000 genomes]
rs4494643	0.83[ASN][1000 genomes]
rs4531834	0.83[ASN][1000 genomes]
rs4986202	0.94[ASN][1000 genomes]
rs748509	0.82[ASN][1000 genomes]
rs7504883	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs751393	0.86[ASN][1000 genomes]
rs892576	0.81[ASN][1000 genomes]
rs919980	0.83[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	nsv833641	chr18:44815063-45020202	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	2 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	chr18:44973600-44976800	Weak transcription	Placenta	Placenta
2	chr18:44975000-44975800	Enhancers	Gastric	stomach
3	chr18:44975400-44975800	Enhancers	Pancreas	Pancrea

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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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