Variant report

Variant	rs9385936
Chromosome Location	chr6:141489301-141489302
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs12174126	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1414120	0.86[ASN][1000 genomes]
rs1452986	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1452993	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1452995	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17070749	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1869273	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2167760	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2184531	0.86[ASN][1000 genomes]
rs57345729	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73776882	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73776884	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73778728	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73778734	0.91[ASN][1000 genomes]
rs73778750	0.86[ASN][1000 genomes]
rs7741795	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9321807	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9373299	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9373301	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9373303	0.91[ASN][1000 genomes]
rs9376580	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9376582	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9376595	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9376596	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9376598	0.91[ASN][1000 genomes]
rs9376604	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9385946	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9385947	0.89[ASN][1000 genomes]
rs9389877	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9389878	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9389880	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9389891	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9389898	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9389899	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9389900	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9389902	0.91[ASN][1000 genomes]
rs9389903	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9399349	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9399351	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9399359	0.86[ASN][1000 genomes]
rs9399360	0.86[ASN][1000 genomes]
rs9403265	0.95[ASN][1000 genomes]
rs9403277	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9403283	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9403285	0.84[ASN][1000 genomes]
rs9403289	0.82[ASN][1000 genomes]
rs967794	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs967795	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs967796	0.87[EUR][1000 genomes];0.94[ASN][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	nsv1019459	chr6:141051249-141862727	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv538453	chr6:141051249-141862727	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv532070	chr6:141057326-141865359	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1025922	chr6:141090901-141865360	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv538454	chr6:141090901-141865360	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1028540	chr6:141121435-141740831	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv604780	chr6:141126080-141740918	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1033387	chr6:141130072-141742682	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1030686	chr6:141130072-141749079	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1024981	chr6:141134064-141742682	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv916684	chr6:141149976-141682411	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv532071	chr6:141150099-141682503	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv1035133	chr6:141156919-141650334	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv1029033	chr6:141156919-141740831	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv886720	chr6:141328865-141725335	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv886721	chr6:141328865-141739208	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
17	nsv1029550	chr6:141372610-142029669	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
18	nsv830822	chr6:141387803-141542998	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv886725	chr6:141428255-141718812	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv886726	chr6:141428255-141764919	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:141475200-141493800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:141480400-141490600	Weak transcription	HSMMtube	muscle
3	chr6:141485400-141492000	Weak transcription	Left Ventricle	heart
4	chr6:141486400-141490600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:141486400-141490800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr6:141486800-141490400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr6:141487000-141490400	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr6:141487000-141490600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr6:141487200-141490400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr6:141487200-141490400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr6:141487200-141490400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr6:141487400-141490600	Weak transcription	Fetal Lung	lung
13	chr6:141487800-141489600	Weak transcription	Ovary	ovary
14	chr6:141489000-141489600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:141489200-141489400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:141489200-141489400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:141489200-141490800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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