Variant report

Variant	rs9969748
Chromosome Location	chr9:110755976-110755977
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10120991	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10124421	0.86[EUR][1000 genomes]
rs10124568	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10816606	0.87[EUR][1000 genomes]
rs10979150	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12002014	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12336889	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12338094	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12338152	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12345583	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12346973	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12352557	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28625170	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28697269	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56065550	0.86[EUR][1000 genomes]
rs73653695	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110749600-110757600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr9:110752400-110757600	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr9:110754800-110757800	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr9:110755000-110757600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:110755200-110756800	Weak transcription	Primary B cells from cord blood	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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