Variant report

Variant	rs9488397
Chromosome Location	chr6:114740063-114740064
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10080647	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10155761	0.96[ASN][1000 genomes]
rs1033885	0.94[JPT][hapmap]
rs10872117	0.83[ASN][1000 genomes]
rs11153481	0.83[ASN][1000 genomes]
rs11962755	0.92[ASN][1000 genomes]
rs11968668	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs12194487	0.81[ASN][1000 genomes]
rs1323046	0.83[ASN][1000 genomes]
rs1323048	0.83[ASN][1000 genomes]
rs1324441	0.94[JPT][hapmap]
rs1324446	0.80[ASN][1000 genomes]
rs1324447	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs1337330	0.80[ASN][1000 genomes]
rs1337335	0.95[ASN][1000 genomes]
rs1337336	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1408452	0.88[JPT][hapmap]
rs1408453	0.88[JPT][hapmap]
rs1408454	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs1415428	0.83[ASN][1000 genomes]
rs1415429	0.83[ASN][1000 genomes]
rs1415430	0.83[ASN][1000 genomes]
rs17326650	0.92[ASN][1000 genomes]
rs1856118	0.92[ASN][1000 genomes]
rs2205734	0.83[ASN][1000 genomes]
rs2205737	0.92[ASN][1000 genomes]
rs2224692	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs2281012	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs2294232	0.85[CHB][hapmap]
rs2349468	0.92[ASN][1000 genomes]
rs2882172	0.92[ASN][1000 genomes]
rs4945515	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs4946001	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs4946003	0.82[JPT][hapmap]
rs56067384	0.92[ASN][1000 genomes]
rs6568839	0.80[ASN][1000 genomes]
rs6902333	0.82[ASN][1000 genomes]
rs6902384	0.82[ASN][1000 genomes]
rs6917878	0.83[ASN][1000 genomes]
rs6919491	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6926249	0.92[ASN][1000 genomes]
rs7749363	0.92[ASN][1000 genomes]
rs7754407	0.80[ASN][1000 genomes]
rs9320491	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9320493	0.86[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs9374461	0.82[ASN][1000 genomes]
rs9374463	0.80[ASN][1000 genomes]
rs9488389	0.87[ASN][1000 genomes]
rs9488390	0.95[ASN][1000 genomes]
rs9488391	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9488404	0.84[JPT][hapmap]
rs9688943	0.84[JPT][hapmap]
rs969877	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34434	chr6:114465305-115462799	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
2	nsv464024	chr6:114489321-114837181	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
3	nsv604544	chr6:114489321-114837181	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
4	esv3692910	chr6:114597419-115480580	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	nsv528128	chr6:114597657-115471129	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
6	nsv818451	chr6:114597657-115471129	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
7	nsv428494	chr6:114666307-114774841	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	esv2758074	chr6:114666308-115526957	Enhancers Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
9	nsv1030191	chr6:114679497-115228028	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	nsv538424	chr6:114679497-115228028	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv1025817	chr6:114715204-115006108	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114720000-114740200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:114738000-114740200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
3	chr6:114739000-114740400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr6:114739400-114740400	Genic enhancers	HUES48 Cell Line	embryonic stem cell
5	chr6:114739400-114740400	Genic enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr6:114739400-114741800	Genic enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:114739400-114742000	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr6:114739600-114740200	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr6:114739600-114740400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr6:114739600-114740600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr6:114739800-114740200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr6:114740000-114740600	Enhancers	HepG2	liver
13	chr6:114740000-114741000	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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