Variant report

Variant	rs72759660
Chromosome Location	chr9:101121164-101121165
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:14)

rs_ID	r²[population]
rs12340823	0.89[ASN][1000 genomes]
rs16915331	0.89[ASN][1000 genomes]
rs17768880	0.89[ASN][1000 genomes]
rs62574339	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62574340	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62574341	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62574342	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62574343	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62574358	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62576560	0.89[ASN][1000 genomes]
rs62576561	0.89[ASN][1000 genomes]
rs650545	1.00[ASN][1000 genomes]
rs72759648	0.89[ASN][1000 genomes]
rs9886874	1.00[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	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv831664	chr9:101024862-101205637	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101118000-101122600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
2	chr9:101118800-101127400	Weak transcription	Brain Germinal Matrix	brain
3	chr9:101118800-101127400	Weak transcription	Fetal Brain Female	brain
4	chr9:101119200-101121200	Enhancers	Muscle Satellite Cultured Cells	--
5	chr9:101119400-101121200	Enhancers	HUVEC	blood vessel
6	chr9:101119600-101121200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr9:101119600-101121200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr9:101120000-101121200	Enhancers	NHDF-Ad	bronchial
9	chr9:101120200-101121200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr9:101120400-101121200	Enhancers	Lung	lung
11	chr9:101120600-101134400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr9:101121000-101121200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:101121000-101123200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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