Variant report

Variant	rs16909618
Chromosome Location	chr9:25700829-25700830
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16909648	1.00[ASN][1000 genomes]
rs16909650	1.00[ASN][1000 genomes]
rs57334759	1.00[ASN][1000 genomes]
rs57381186	1.00[ASN][1000 genomes]
rs58555020	1.00[ASN][1000 genomes]
rs60016118	1.00[ASN][1000 genomes]
rs60085074	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61607792	1.00[ASN][1000 genomes]
rs7020692	0.94[YRI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7021695	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7037003	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73644579	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7850994	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869035	chr9:25287213-25779281	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv531597	chr9:25325401-25779422	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv613912	chr9:25538362-25722614	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv533233	chr9:25548163-25702906	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv831530	chr9:25563811-25754022	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1015883	chr9:25633359-26315286	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 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	chr9:25696000-25703800	Weak transcription	Fetal Lung	lung
2	chr9:25700000-25701800	Enhancers	Hela-S3	cervix
3	chr9:25700400-25701600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:25700600-25701000	Enhancers	NH-A	brain
5	chr9:25700600-25701000	Enhancers	Osteobl	bone
6	chr9:25700600-25701200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:25700600-25701200	Enhancers	NHEK	skin
8	chr9:25700600-25701800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr9:25700600-25701800	Enhancers	Muscle Satellite Cultured Cells	--
10	chr9:25700600-25701800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:25700600-25702200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr9:25700800-25702000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr9:25700800-25703000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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