Variant report

Variant	rs678363
Chromosome Location	chr9:97295486-97295487
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10115929	0.86[ASN][1000 genomes]
rs10119223	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10119419	0.86[ASN][1000 genomes]
rs10733753	0.86[ASN][1000 genomes]
rs10761331	0.86[ASN][1000 genomes]
rs10761332	0.86[ASN][1000 genomes]
rs10761333	0.86[ASN][1000 genomes]
rs10821364	0.85[ASN][1000 genomes]
rs10821365	0.86[ASN][1000 genomes]
rs10821367	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs10821369	0.84[ASN][1000 genomes]
rs10993226	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10993241	0.95[CHB][hapmap];0.87[ASN][1000 genomes]
rs10993242	0.91[CHB][hapmap];0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs11790263	0.86[ASN][1000 genomes]
rs12551995	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12552009	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12552912	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2280300	0.95[CHB][hapmap];0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs2679602	0.84[CEU][hapmap];0.95[CHB][hapmap]
rs2679611	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2772013	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2790400	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2790404	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2945802	0.95[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2987882	0.84[CEU][hapmap];0.95[CHB][hapmap]
rs2987886	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987887	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2987888	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987889	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2993973	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2993975	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3864788	0.86[ASN][1000 genomes]
rs4291336	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4743956	0.83[EUR][1000 genomes]
rs4744349	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4744353	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs488270	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs491123	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs497361	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs504644	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs514222	0.83[CEU][hapmap];0.95[CHB][hapmap]
rs518768	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs540124	0.95[CEU][hapmap];0.83[CHB][hapmap]
rs543698	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs543731	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs547693	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs549615	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs572689	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs573371	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs573847	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs576745	0.82[CHB][hapmap]
rs605323	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs606207	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs607160	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs608837	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs652867	0.80[EUR][1000 genomes]
rs663092	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs669113	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs688843	0.96[CEU][hapmap];0.95[CHB][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs693399	0.84[CEU][hapmap];0.95[CHB][hapmap]
rs7024700	1.00[CEU][hapmap];0.86[CHB][hapmap];0.88[EUR][1000 genomes]
rs7048277	0.86[ASN][1000 genomes]
rs781650	0.95[CEU][hapmap];0.95[CHB][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7867912	0.85[ASN][1000 genomes]
rs802918	0.81[CHB][hapmap]
rs802919	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9409801	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs965474	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs9696211	0.83[ASN][1000 genomes]
rs9696774	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761545	chr9:97025298-97356950	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1041195	chr9:97054795-97402378	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	esv1840205	chr9:97202200-97366400	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv893595	chr9:97268182-97330693	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv525298	chr9:97289583-97312584	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97293800-97296200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr9:97295000-97297200	Enhancers	Fetal Intestine Large	intestine
3	chr9:97295000-97297200	Enhancers	Fetal Intestine Small	intestine
4	chr9:97295200-97296200	Flanking Active TSS	HepG2	liver
5	chr9:97295200-97296400	Enhancers	Liver	Liver
6	chr9:97295200-97297200	Enhancers	Fetal Kidney	kidney
7	chr9:97295400-97295800	Active TSS	Duodenum Mucosa	Duodenum
8	chr9:97295400-97295800	Active TSS	Rectal Mucosa Donor 29	rectum
9	chr9:97295400-97295800	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr9:97295400-97296000	Enhancers	Pancreas	Pancrea
11	chr9:97295400-97296000	Enhancers	A549	lung
12	chr9:97295400-97296200	Enhancers	Stomach Mucosa	stomach

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