Variant report

Variant	rs6784156
Chromosome Location	chr3:121038805-121038806
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10934551	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs11709726	1.00[JPT][hapmap]
rs11713643	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs1191288	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1191290	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1191293	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1191296	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1191297	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1191300	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1191309	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1211513	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12487633	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12488196	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13077305	1.00[CHB][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap]
rs13097659	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs13434156	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1381057	1.00[CHB][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap]
rs1381058	1.00[JPT][hapmap]
rs1381059	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs1397824	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1511432	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1588538	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17195196	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs173087	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1795387	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1795390	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1795392	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1795404	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1987098	0.81[AMR][1000 genomes]
rs2030531	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2126139	0.82[AMR][1000 genomes]
rs2141658	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2331709	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs234997	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2656043	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2656048	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2701057	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3218649	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs338958	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs338959	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs338969	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs338973	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs338979	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs338981	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs338983	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs338986	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs338994	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs338996	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs339000	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs339006	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs339011	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3732406	1.00[JPT][hapmap]
rs3772122	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs3911713	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs3914744	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4048751	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4107754	0.85[AMR][1000 genomes]
rs4346498	0.85[AMR][1000 genomes]
rs4555467	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs4676677	1.00[CHB][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap]
rs4676719	0.85[AMR][1000 genomes]
rs60648200	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6438630	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6438633	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs6769377	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs6775508	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6782025	0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap]
rs6782033	0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap]
rs6787048	0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap]
rs6793029	0.83[AMR][1000 genomes]
rs6793252	1.00[CHB][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap]
rs6797376	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs6798699	1.00[JPT][hapmap]
rs6806191	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs693403	0.87[ASW][hapmap];0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.86[MKK][hapmap];0.84[YRI][hapmap]
rs7609781	0.82[AMR][1000 genomes]
rs7615529	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs7615712	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7621376	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs7627978	0.82[AMR][1000 genomes]
rs7632907	0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap]
rs7634611	0.82[AMR][1000 genomes]
rs7635903	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7645027	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs7645849	0.85[AMR][1000 genomes]
rs7648360	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7650439	0.83[AMR][1000 genomes]
rs7650658	0.81[AMR][1000 genomes]
rs9849118	0.82[AMR][1000 genomes]
rs9860056	0.87[AMR][1000 genomes];0.90[EUR][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	nsv869548	chr3:120320731-121076337	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1005275	chr3:120700604-121102735	Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv998555	chr3:120700604-121348015	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
4	nsv1008441	chr3:120730017-121102735	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
5	nsv536709	chr3:120730017-121102735	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
6	nsv829701	chr3:120935402-121115932	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv521397	chr3:120970900-121192350	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv591395	chr3:120970900-121501070	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv591396	chr3:120970900-121557533	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
10	nsv591397	chr3:120977383-121505882	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs6784156	PARP15	cis	parietal	SCAN
rs6784156	CHST13	cis	parietal	SCAN
rs6784156	STXBP5L	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121033600-121052200	Weak transcription	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links