Variant report

Variant	rs4547912
Chromosome Location	chr5:93571190-93571191
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 133 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:124)

rs_ID	r²[population]
rs10035340	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10036829	0.90[AMR][1000 genomes]
rs10040648	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10044066	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10044139	0.90[AMR][1000 genomes]
rs10050465	0.90[AMR][1000 genomes]
rs10055340	0.90[AMR][1000 genomes]
rs10055741	0.90[AMR][1000 genomes]
rs10055994	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10057605	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10057814	0.90[AMR][1000 genomes]
rs10059230	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10060160	0.93[AMR][1000 genomes]
rs10061080	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10061099	0.90[AMR][1000 genomes]
rs10062711	0.90[AMR][1000 genomes]
rs10063612	0.90[AMR][1000 genomes]
rs10064520	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10065056	0.86[AMR][1000 genomes]
rs10066791	0.90[AMR][1000 genomes]
rs10070390	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10072232	0.90[AMR][1000 genomes]
rs10072592	0.93[AMR][1000 genomes]
rs10076052	0.90[AMR][1000 genomes]
rs10076192	0.93[AMR][1000 genomes]
rs10078194	0.86[AMR][1000 genomes]
rs10440717	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10476596	0.93[AMR][1000 genomes]
rs10476597	0.93[AMR][1000 genomes]
rs10476598	0.90[AMR][1000 genomes]
rs10476599	0.90[AMR][1000 genomes]
rs10476601	0.90[AMR][1000 genomes]
rs10476602	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10514380	0.86[AMR][1000 genomes]
rs10514382	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12109629	0.90[AMR][1000 genomes]
rs12152763	0.93[AMR][1000 genomes]
rs12153501	0.90[AMR][1000 genomes]
rs12153506	0.90[AMR][1000 genomes]
rs12153788	0.90[AMR][1000 genomes]
rs12187701	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12188453	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12189466	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12374432	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12374463	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12374470	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12374488	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12716456	0.90[AMR][1000 genomes]
rs12716457	0.90[AMR][1000 genomes]
rs12716460	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12716462	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13153245	0.90[AMR][1000 genomes]
rs13154249	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13156002	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13156865	0.86[AMR][1000 genomes]
rs13163610	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13165147	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13169675	0.93[AMR][1000 genomes]
rs13170509	0.90[AMR][1000 genomes]
rs13173952	0.86[AMR][1000 genomes]
rs13174700	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13177800	0.93[AMR][1000 genomes]
rs13181660	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13185608	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13185660	0.90[AMR][1000 genomes]
rs13186579	0.84[AMR][1000 genomes]
rs13356088	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17083455	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17315943	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17323433	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17374627	0.93[AMR][1000 genomes]
rs17376207	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17376456	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2085960	0.90[AMR][1000 genomes]
rs2290937	0.81[AMR][1000 genomes]
rs28539612	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs28575883	0.90[AMR][1000 genomes]
rs28633397	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28637444	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34013242	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34068652	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34138834	0.86[AMR][1000 genomes]
rs34184666	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34384674	0.84[AMR][1000 genomes]
rs34595581	0.90[AMR][1000 genomes]
rs34673483	0.86[AMR][1000 genomes]
rs34717672	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34756085	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34854140	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs35075119	0.86[AMR][1000 genomes]
rs35184505	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35747258	0.90[AMR][1000 genomes]
rs36026719	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs36091096	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3940842	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55832164	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56046246	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs56373208	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58734583	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59472588	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61132622	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs66696214	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs66978370	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs67066109	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6867042	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs71641007	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72788365	0.86[AMR][1000 genomes]
rs7701011	0.86[AMR][1000 genomes]
rs7701974	0.90[AMR][1000 genomes]
rs7702521	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7718842	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7728736	0.90[AMR][1000 genomes]
rs7734897	0.86[AMR][1000 genomes]
rs7736620	0.86[AMR][1000 genomes]
rs9314092	0.90[AMR][1000 genomes]
rs9314093	0.84[AMR][1000 genomes]
rs9314095	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9314096	0.84[AMR][1000 genomes]
rs9314099	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9314100	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9314102	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9885329	0.93[AMR][1000 genomes]
rs9968691	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9968749	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532196	chr5:92933949-93573527	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1023191	chr5:93351646-93947928	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv537808	chr5:93351646-93947928	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers 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	17 gene(s)	inside rSNPs	diseases
4	esv2753025	chr5:93356544-93812844	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv530552	chr5:93416111-93588509	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv1024014	chr5:93460441-93655609	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv830406	chr5:93514329-93683512	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv3514690	chr5:93569039-93573268	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
9	esv3514691	chr5:93569039-93573268	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:93553200-93576600	Weak transcription	Hela-S3	cervix
2	chr5:93555600-93578800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr5:93568000-93617200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr5:93569200-93572400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:93570200-93571400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr5:93570200-93572000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
7	chr5:93570400-93572200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
8	chr5:93570400-93572200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
9	chr5:93570800-93571600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr5:93571000-93571200	Flanking Active TSS	Liver	Liver
11	chr5:93571000-93571600	ZNF genes & repeats	Brain Germinal Matrix	brain
12	chr5:93571000-93572200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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