Variant report

Variant	rs4977476
Chromosome Location	chr9:18948086-18948087
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 106 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs1006120	0.87[CHB][hapmap];0.91[CHD][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs10738524	0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs10757004	0.95[CHB][hapmap];0.83[CHD][hapmap];0.84[ASN][1000 genomes]
rs10757007	0.80[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap];0.83[MEX][hapmap];0.90[ASN][1000 genomes]
rs10757008	0.80[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap];0.83[MEX][hapmap];0.90[ASN][1000 genomes]
rs10757009	0.90[ASN][1000 genomes]
rs10757010	0.90[ASN][1000 genomes]
rs10757011	0.91[CHB][hapmap];0.86[CHD][hapmap];0.80[JPT][hapmap]
rs10757012	0.93[ASN][1000 genomes]
rs10757016	0.91[CHB][hapmap]
rs10757018	0.85[CHB][hapmap]
rs10811069	0.84[ASN][1000 genomes]
rs10811080	0.81[CHD][hapmap]
rs10811085	0.82[CHB][hapmap]
rs10811092	0.82[CHB][hapmap]
rs10811099	0.86[CHB][hapmap]
rs10963863	0.91[CHB][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs10963869	0.86[ASN][1000 genomes]
rs10963896	0.82[CHB][hapmap]
rs10963898	0.81[CHD][hapmap]
rs10963907	0.86[CHB][hapmap]
rs10963910	0.82[CHB][hapmap]
rs10963911	0.82[CHB][hapmap]
rs10963912	0.81[CHB][hapmap]
rs12553946	0.86[CHB][hapmap]
rs12686643	0.87[ASN][1000 genomes]
rs1327502	0.84[ASN][1000 genomes]
rs17236081	0.86[CHB][hapmap]
rs1887444	0.80[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap];0.83[MEX][hapmap];0.90[ASN][1000 genomes]
rs1887445	0.90[ASN][1000 genomes]
rs1932445	0.83[CHB][hapmap];0.86[CHD][hapmap]
rs1932448	0.83[CHB][hapmap];0.95[CHD][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs1932452	0.86[CHB][hapmap]
rs1932453	0.86[CHB][hapmap]
rs1977444	0.91[CHB][hapmap];0.93[CHD][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs2039008	0.87[CHB][hapmap];0.87[ASN][1000 genomes]
rs2039010	0.87[CHB][hapmap];0.91[CHD][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs2039011	0.83[CHB][hapmap];0.80[ASN][1000 genomes]
rs2184656	0.81[CHB][hapmap]
rs2291503	0.82[CHB][hapmap]
rs36098671	0.81[ASN][1000 genomes]
rs3892045	0.86[CHB][hapmap]
rs4395970	0.91[CHB][hapmap]
rs4419893	0.91[CHD][hapmap];0.85[ASN][1000 genomes]
rs4977269	0.87[ASN][1000 genomes]
rs4977270	0.87[ASN][1000 genomes]
rs4977273	0.87[CHB][hapmap];0.90[CHD][hapmap];0.83[ASN][1000 genomes]
rs4977477	0.95[CHB][hapmap];0.85[JPT][hapmap];0.90[ASN][1000 genomes]
rs4977478	0.87[ASN][1000 genomes]
rs4977479	0.85[ASN][1000 genomes]
rs4977482	0.83[CHD][hapmap]
rs6475272	0.83[CEU][hapmap];0.91[CHB][hapmap];0.91[CHD][hapmap];0.85[JPT][hapmap];0.87[MEX][hapmap];0.92[ASN][1000 genomes]
rs6475273	0.91[CHB][hapmap];0.91[CHD][hapmap];0.80[JPT][hapmap];0.87[MEX][hapmap];0.90[ASN][1000 genomes]
rs6475274	0.86[CHB][hapmap];0.89[ASN][1000 genomes]
rs6475275	0.87[CHB][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs6475276	0.87[CHB][hapmap];0.91[CHD][hapmap];0.80[JPT][hapmap];0.85[ASN][1000 genomes]
rs6475277	0.87[ASN][1000 genomes]
rs6475279	0.85[CHB][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs6475292	0.94[ASN][1000 genomes]
rs6475293	0.87[ASN][1000 genomes]
rs6475294	0.83[CHB][hapmap];0.95[CHD][hapmap];0.86[ASN][1000 genomes]
rs6475295	0.91[CHB][hapmap];0.98[CHD][hapmap];0.90[JPT][hapmap];0.82[MEX][hapmap];0.93[ASN][1000 genomes]
rs6475296	0.83[CHB][hapmap];0.98[CHD][hapmap];0.83[ASN][1000 genomes]
rs6475297	0.83[CHB][hapmap];0.83[ASN][1000 genomes]
rs7021572	0.84[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[JPT][hapmap];0.83[MEX][hapmap];0.90[ASN][1000 genomes]
rs7024697	0.82[CHB][hapmap]
rs7025581	0.89[ASN][1000 genomes]
rs7028706	0.83[CEU][hapmap];0.86[CHB][hapmap];0.86[CHD][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs7028858	0.82[CHB][hapmap]
rs7028936	0.82[CHB][hapmap]
rs7030791	0.81[CHB][hapmap]
rs7034201	0.83[CHB][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs7037837	0.82[CHB][hapmap]
rs7038730	0.82[CHB][hapmap];0.81[CHD][hapmap]
rs7041732	0.90[ASN][1000 genomes]
rs7042382	0.81[CHB][hapmap]
rs7044864	0.86[CHB][hapmap];0.86[CHD][hapmap];0.82[ASN][1000 genomes]
rs7045059	0.95[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs7045203	0.86[CEU][hapmap];0.91[CHB][hapmap];0.85[JPT][hapmap];0.92[ASN][1000 genomes]
rs7048198	0.95[CHB][hapmap];0.85[JPT][hapmap];0.90[ASN][1000 genomes]
rs7848918	0.87[CHB][hapmap];0.91[CHD][hapmap]
rs7849807	0.95[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs7852907	0.81[CHB][hapmap]
rs7856117	0.91[CHB][hapmap];0.98[CHD][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs7857590	0.82[CHB][hapmap];0.81[CHD][hapmap]
rs7862694	0.86[CHB][hapmap]
rs7864376	0.82[CHB][hapmap]
rs7865237	0.95[CHB][hapmap];0.85[JPT][hapmap];0.90[ASN][1000 genomes]
rs7865461	0.91[CHB][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs7871450	0.93[ASN][1000 genomes]
rs7871456	0.86[CHB][hapmap];0.90[CHD][hapmap];0.80[JPT][hapmap];0.86[ASN][1000 genomes]
rs7871732	0.86[ASN][1000 genomes]
rs883439	0.86[CHB][hapmap]
rs9298798	0.82[CHB][hapmap]
rs953734	0.87[CHB][hapmap];0.88[CHD][hapmap];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv525659	chr9:18288212-19009041	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1019127	chr9:18288271-18996288	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv892692	chr9:18519699-19045502	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv949111	chr9:18758205-18994588	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
6	nsv1017820	chr9:18882219-19587377	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
7	nsv540078	chr9:18882219-19587377	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
8	nsv466282	chr9:18920357-18960393	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv471289	chr9:18920357-18960393	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv613727	chr9:18920357-18960393	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv892699	chr9:18945868-19025693	Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4977476	PLIN2	cis	lymphoblastoid	seeQTL
rs4977476	ADFP	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18946000-18952800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:18947400-18948400	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr9:18947400-18948800	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr9:18947800-18948200	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr9:18947800-18948200	Enhancers	Fetal Thymus	thymus

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