Variant report

Variant	rs11788619
Chromosome Location	chr9:22258082-22258083
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11790403	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56752882	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62559497	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62559498	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62559499	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62559500	0.89[EUR][1000 genomes]
rs62559501	1.00[ASN][1000 genomes]
rs62559502	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62559503	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62559504	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62559505	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62559506	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62559507	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62559508	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62559524	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7032094	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7872733	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529609	chr9:21708371-22537069	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv531617	chr9:21985057-22809676	Genic enhancers Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv1021264	chr9:22159622-22293804	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1033789	chr9:22183150-22266091	Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1029289	chr9:22193167-23023688	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv1016067	chr9:22210874-22432654	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1015364	chr9:22211364-22416886	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv540086	chr9:22211364-22416886	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv1023972	chr9:22246764-22426267	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv540087	chr9:22246764-22426267	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:22256400-22259200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:22256400-22259400	Enhancers	HMEC	breast
3	chr9:22256600-22259000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr9:22257000-22258200	Enhancers	Placenta	Placenta
5	chr9:22257000-22259200	Enhancers	NHEK	skin
6	chr9:22257200-22260200	Weak transcription	A549	lung
7	chr9:22257200-22261600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr9:22257600-22258200	Enhancers	Esophagus	oesophagus
9	chr9:22257600-22259400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
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