Variant report

Variant	rs6791672
Chromosome Location	chr3:112591392-112591393
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1016348	0.85[ASN][1000 genomes]
rs10934190	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10934192	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10934193	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12497951	0.86[ASN][1000 genomes]
rs13326243	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1392786	0.83[ASN][1000 genomes]
rs1466872	0.84[ASN][1000 genomes]
rs1500878	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1500879	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1971986	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2101440	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2171509	0.85[ASN][1000 genomes]
rs2399436	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2399443	0.98[ASN][1000 genomes]
rs28859668	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28867393	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4103791	0.86[ASN][1000 genomes]
rs4234417	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4478054	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4571210	0.85[EUR][1000 genomes]
rs4682120	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4682125	0.86[ASN][1000 genomes]
rs4682440	0.98[ASN][1000 genomes]
rs4682441	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4682444	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6438111	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6438112	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6438113	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6438114	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6438118	0.85[ASN][1000 genomes]
rs6438119	0.85[ASN][1000 genomes]
rs6438120	0.84[ASN][1000 genomes]
rs6438122	0.83[ASN][1000 genomes]
rs6765379	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6766388	0.98[ASN][1000 genomes]
rs6769091	0.86[ASN][1000 genomes]
rs6772799	0.85[ASN][1000 genomes]
rs6784838	0.86[ASN][1000 genomes]
rs6791158	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6808249	0.82[ASN][1000 genomes]
rs7355890	0.84[ASN][1000 genomes]
rs7611690	0.85[ASN][1000 genomes]
rs7615462	0.86[ASN][1000 genomes]
rs7622812	0.85[ASN][1000 genomes]
rs7622814	0.83[ASN][1000 genomes]
rs7632218	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7646849	0.86[ASN][1000 genomes]
rs7652504	0.85[ASN][1000 genomes]
rs7652536	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9815606	0.85[ASN][1000 genomes]
rs9818564	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9819079	0.82[ASN][1000 genomes]
rs9823363	0.86[ASN][1000 genomes]
rs9826308	0.85[ASN][1000 genomes]
rs9833991	0.86[ASN][1000 genomes]
rs9834353	0.85[ASN][1000 genomes]
rs9834840	0.86[ASN][1000 genomes]
rs9838082	0.80[EUR][1000 genomes]
rs9847365	0.98[ASN][1000 genomes]
rs9854885	0.86[ASN][1000 genomes]
rs9864295	0.84[ASN][1000 genomes]
rs9865242	0.85[ASN][1000 genomes]
rs9868053	0.85[ASN][1000 genomes]
rs9868839	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9870335	0.86[ASN][1000 genomes]
rs9870568	0.85[ASN][1000 genomes]
rs9871985	0.86[ASN][1000 genomes]
rs9875551	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9877631	0.86[ASN][1000 genomes]
rs9883255	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[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	esv3329419	chr3:112236688-112620544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv432477	chr3:112390310-112603310	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3431441	chr3:112453467-113213252	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv877343	chr3:112470586-112597706	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv3501334	chr3:112546820-112648766	Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv3501335	chr3:112546820-112648766	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112590600-112593600	Enhancers	Primary B cells from peripheral blood	blood
2	chr3:112590600-112593800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr3:112590800-112592200	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr3:112591000-112592800	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr3:112591000-112592800	Enhancers	Primary B cells from cord blood	blood
6	chr3:112591200-112591800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr3:112591200-112592200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr3:112591200-112592400	Enhancers	HUES48 Cell Line	embryonic stem cell

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