Variant report

Variant	rs2157059
Chromosome Location	chr3:46358904-46358905
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10865940	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11130089	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11711054	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11923720	0.80[AMR][1000 genomes]
rs13081845	0.81[EUR][1000 genomes]
rs13096142	0.80[EUR][1000 genomes]
rs1799865	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2097282	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2097284	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2157057	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2157058	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2187669	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2187670	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2213291	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2213292	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3092963	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3138042	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34148191	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34193387	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34505903	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34997146	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35053103	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35465430	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35510257	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35675823	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35971655	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36030342	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs36048784	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs3918358	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4134396	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4683198	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4683211	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs4683215	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4683218	0.82[ASN][1000 genomes]
rs62244813	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs62244827	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62244828	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62244840	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62244848	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6441953	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6441958	0.80[ASN][1000 genomes]
rs6441959	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6441960	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6441961	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6441962	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6441963	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6441964	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6441972	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6767895	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6771900	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6775208	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6783993	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6785878	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6785981	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6788723	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6794300	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71615444	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7372094	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7374654	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7374671	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7432080	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7612940	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7626249	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs762789	0.80[ASN][1000 genomes]
rs7634816	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7635588	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs963045	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9813756	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9818053	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9852052	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9856098	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9875668	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876734	chr3:45725031-46468467	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv3323840	chr3:46352348-46497196	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3389382	chr3:46352798-46496696	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46350800-46367600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr3:46355000-46359600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr3:46355600-46362000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr3:46356000-46359800	Enhancers	Primary B cells from peripheral blood	blood
5	chr3:46357600-46363400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr3:46358400-46361800	Weak transcription	Primary B cells from cord blood	blood
7	chr3:46358800-46360200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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