Variant report

Variant	rs73137393
Chromosome Location	chr3:89471701-89471702
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1028013	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1054750	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1157607	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1157608	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12152372	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12629165	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12629758	0.82[AMR][1000 genomes]
rs12631313	0.86[EUR][1000 genomes]
rs12634269	0.83[EUR][1000 genomes]
rs12634341	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12636710	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12639506	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1499780	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1512183	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1512185	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17026944	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17801380	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1912965	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1912966	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2048519	0.80[AMR][1000 genomes]
rs2117138	0.84[EUR][1000 genomes]
rs2346836	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2346840	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28623022	0.81[ASN][1000 genomes]
rs2881488	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3762717	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs57670516	0.81[ASN][1000 genomes]
rs59541469	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs60759140	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62275018	0.81[ASN][1000 genomes]
rs62275019	0.81[ASN][1000 genomes]
rs6551412	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs66708608	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6782527	0.85[ASN][1000 genomes]
rs6795074	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6800041	0.81[ASN][1000 genomes]
rs6800436	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73137381	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73137382	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73137384	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73137387	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73137395	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73139104	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73139105	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73139110	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73139115	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73139117	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73139118	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73139119	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73139121	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73139125	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73139127	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73139129	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73139131	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73139133	0.82[EUR][1000 genomes]
rs73139134	0.81[EUR][1000 genomes]
rs73139135	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73139139	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73139144	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73139147	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73139148	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73139257	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73139261	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73139276	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73139281	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73139284	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73139286	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73139288	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73139290	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73139296	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73139302	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73141104	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73141108	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73141113	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73145303	0.81[AMR][1000 genomes]
rs73145305	0.81[AMR][1000 genomes]
rs73146907	0.82[AMR][1000 genomes]
rs73146968	0.82[AMR][1000 genomes]
rs73146970	0.82[AMR][1000 genomes]
rs73149113	0.82[AMR][1000 genomes]
rs7615949	0.81[ASN][1000 genomes]
rs7616322	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7626735	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7645408	0.83[ASN][1000 genomes]
rs7650466	0.86[EUR][1000 genomes]
rs972030	0.82[AMR][1000 genomes]
rs9844971	0.81[ASN][1000 genomes]
rs9849029	0.81[ASN][1000 genomes]
rs9854073	0.81[ASN][1000 genomes]
rs9864984	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv437866	chr3:89247881-89480265	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1008018	chr3:89382031-90254063	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv536639	chr3:89382031-90254063	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1010932	chr3:89424428-90192503	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:89460800-89521200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr3:89463800-89478600	Weak transcription	Fetal Brain Female	brain
3	chr3:89465200-89471800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:89467800-89472600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:89469400-89483400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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