Variant report

Variant	rs6532332
Chromosome Location	chr4:92550838-92550839
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1003265	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10470887	0.83[ASN][1000 genomes]
rs10470940	0.86[ASN][1000 genomes]
rs1114625	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11721769	0.80[ASN][1000 genomes]
rs11731403	0.82[EUR][1000 genomes]
rs11931400	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11932865	0.81[EUR][1000 genomes]
rs11941047	0.85[ASN][1000 genomes]
rs11941720	0.82[EUR][1000 genomes]
rs11941818	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11945625	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11946091	0.83[EUR][1000 genomes]
rs11946281	0.82[EUR][1000 genomes]
rs12501164	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13111039	0.82[ASN][1000 genomes]
rs13111521	0.86[ASN][1000 genomes]
rs13135264	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13135497	0.84[ASN][1000 genomes]
rs1356289	0.83[ASN][1000 genomes]
rs1516705	0.89[ASN][1000 genomes]
rs1533459	0.85[ASN][1000 genomes]
rs1533460	0.85[ASN][1000 genomes]
rs1533462	0.82[EUR][1000 genomes]
rs1607078	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17220140	0.85[ASN][1000 genomes]
rs17285646	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17841804	0.80[EUR][1000 genomes]
rs1914238	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1914239	0.83[EUR][1000 genomes]
rs28840497	0.83[ASN][1000 genomes]
rs34451329	0.80[EUR][1000 genomes]
rs34920942	0.80[EUR][1000 genomes]
rs34940074	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34982476	0.81[EUR][1000 genomes]
rs4348056	0.81[ASN][1000 genomes]
rs4376107	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4472103	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57015636	0.82[ASN][1000 genomes]
rs61143842	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62311884	0.81[EUR][1000 genomes]
rs62311910	0.80[EUR][1000 genomes]
rs6532326	0.83[ASN][1000 genomes]
rs6532334	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6532335	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6821624	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6822174	0.81[EUR][1000 genomes]
rs6823252	0.82[EUR][1000 genomes]
rs6834624	0.89[ASN][1000 genomes]
rs6837847	0.83[ASN][1000 genomes]
rs6841299	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6841361	0.82[EUR][1000 genomes]
rs6852718	0.82[EUR][1000 genomes]
rs7664136	0.84[ASN][1000 genomes]
rs7681874	0.83[ASN][1000 genomes]
rs7687544	0.86[ASN][1000 genomes]
rs7687911	0.82[ASN][1000 genomes]
rs7695161	0.84[ASN][1000 genomes]
rs9918048	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869023	chr4:91940838-92935383	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv879576	chr4:92356118-92651110	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv879580	chr4:92373327-92551065	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv594861	chr4:92379081-92898309	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv948428	chr4:92382683-93161851	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv594862	chr4:92392152-93222515	Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv461585	chr4:92395356-92761582	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv594863	chr4:92395356-92761582	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv999961	chr4:92396538-93213898	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv537178	chr4:92396538-93213898	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
11	nsv533406	chr4:92396539-93184304	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	nsv530154	chr4:92396539-93359983	Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1006366	chr4:92481747-92755677	Enhancers Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv1003269	chr4:92488825-92758977	Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv869490	chr4:92506402-93219336	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
16	nsv999701	chr4:92518040-93233556	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv537180	chr4:92518040-93233556	Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv530442	chr4:92528849-93184304	Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
19	esv3427021	chr4:92534823-92558935	ZNF genes & repeats Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3401040	chr4:92534823-92561189	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:92546800-92552600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr4:92548800-92551200	Strong transcription	H1 Cell Line	embryonic stem cell
3	chr4:92548800-92552600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:92549000-92556200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr4:92549000-92557000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr4:92549800-92551800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:92550600-92551400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
8	chr4:92550800-92551000	Genic enhancers	H9 Cell Line	embryonic stem cell
9	chr4:92550800-92551000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
10	chr4:92550800-92551400	Strong transcription	HUES48 Cell Line	embryonic stem cell

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