Variant report

Variant	rs4506313
Chromosome Location	chr9:18990027-18990028
allele	C/T
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]
rs10116436	0.87[ASN][1000 genomes]
rs10121747	0.85[ASN][1000 genomes]
rs10122088	0.81[JPT][hapmap]
rs10125038	0.87[ASN][1000 genomes]
rs10757004	0.83[CHB][hapmap]
rs10757007	0.83[CHB][hapmap]
rs10757008	0.83[CHB][hapmap]
rs10757016	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs10757018	0.82[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs10757021	0.81[ASN][1000 genomes]
rs10757022	0.82[CHB][hapmap]
rs10811073	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10811074	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10811075	0.91[CHB][hapmap];0.86[JPT][hapmap];0.89[ASN][1000 genomes]
rs10811076	0.90[ASN][1000 genomes]
rs10811078	0.88[ASN][1000 genomes]
rs10811079	0.88[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs10811080	0.91[CHB][hapmap];0.80[CHD][hapmap];0.86[JPT][hapmap];0.89[ASN][1000 genomes]
rs10811081	0.88[ASN][1000 genomes]
rs10811082	0.91[CHB][hapmap];0.86[JPT][hapmap];0.89[ASN][1000 genomes]
rs10811083	0.89[ASN][1000 genomes]
rs10811084	0.89[ASN][1000 genomes]
rs10811085	0.95[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs10811092	0.85[JPT][hapmap]
rs10811099	0.83[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs10811100	0.81[ASN][1000 genomes]
rs10963894	0.90[ASN][1000 genomes]
rs10963896	0.95[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs10963897	0.95[CHB][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs10963898	0.91[CHB][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs10963907	0.83[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs10963910	0.90[JPT][hapmap]
rs10963911	0.90[JPT][hapmap]
rs11790123	0.91[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs12352657	0.91[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs12352756	0.91[CHB][hapmap];0.89[ASN][1000 genomes]
rs12553946	0.83[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs13284512	0.80[ASN][1000 genomes]
rs17236081	0.83[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs1887444	0.83[CHB][hapmap]
rs1932445	0.86[CHB][hapmap]
rs1932447	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1932452	0.83[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs1932453	0.83[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs2152463	0.88[ASN][1000 genomes]
rs2152464	0.91[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs2184656	0.95[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs2383082	0.87[ASN][1000 genomes]
rs2383083	0.87[ASN][1000 genomes]
rs3892045	0.83[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs4130084	0.83[ASN][1000 genomes]
rs4395970	0.87[CHB][hapmap];0.91[JPT][hapmap]
rs4977273	0.82[CHB][hapmap]
rs4977477	0.83[CHB][hapmap]
rs62560430	0.80[ASN][1000 genomes]
rs6475295	0.86[CHB][hapmap]
rs6475299	0.86[CHB][hapmap];0.85[JPT][hapmap];0.90[YRI][hapmap];0.85[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs6475300	0.86[CHB][hapmap];0.85[JPT][hapmap];0.90[YRI][hapmap];0.85[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs6475303	0.84[ASN][1000 genomes]
rs6475304	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6475305	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6475306	0.87[ASN][1000 genomes]
rs66688010	0.80[ASN][1000 genomes]
rs7020294	0.89[ASN][1000 genomes]
rs7021572	0.83[CHB][hapmap]
rs7022960	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7024697	0.95[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs7025123	0.91[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs7028858	0.95[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs7028936	0.95[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs7029677	0.81[ASN][1000 genomes]
rs7037837	0.91[CHB][hapmap];0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs7038730	0.83[ASW][hapmap];0.95[CHB][hapmap];0.80[CHD][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs7045059	0.83[CHB][hapmap]
rs7048198	0.83[CHB][hapmap]
rs7848929	0.89[ASN][1000 genomes]
rs7849807	0.83[CHB][hapmap]
rs7852907	0.95[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs7856117	0.86[CHB][hapmap]
rs7857590	0.95[CHB][hapmap];0.80[CHD][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs7858618	0.83[CHD][hapmap]
rs7862694	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs7864376	0.95[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs7864909	0.87[ASN][1000 genomes]
rs7864930	0.88[ASN][1000 genomes]
rs7865237	0.83[CHB][hapmap]
rs7867428	0.90[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs7870547	0.90[ASN][1000 genomes]
rs7871030	0.85[ASN][1000 genomes]
rs7871205	0.90[CHB][hapmap];0.85[ASN][1000 genomes]
rs7871456	0.91[CHB][hapmap]
rs7871505	0.86[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs7875035	0.86[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs883439	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs953734	0.82[CHB][hapmap]

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	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
9	nsv1022697	chr9:18951530-19010894	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv892700	chr9:18979441-19156784	Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
11	esv1799697	chr9:18988418-18996642	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4506313	ADFP	Cis_1M	lymphoblastoid	RTeQTL
rs4506313	PLIN2	cis	lymphoblastoid	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18985800-18991800	Weak transcription	Pancreas	Pancrea
2	chr9:18985800-18993400	Weak transcription	Fetal Thymus	thymus
3	chr9:18987400-18993600	Weak transcription	Fetal Kidney	kidney
4	chr9:18989800-18990200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr9:18990000-18994200	Weak transcription	Fetal Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links