Variant report

Variant	rs58630597
Chromosome Location	chr6:141468712-141468713
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1037440	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1037441	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10440884	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12111539	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12664383	0.83[EUR][1000 genomes]
rs13192943	0.83[EUR][1000 genomes]
rs13209869	0.83[EUR][1000 genomes]
rs13209897	0.83[EUR][1000 genomes]
rs13211842	0.84[EUR][1000 genomes]
rs1377322	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1377323	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1545513	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17070752	0.82[EUR][1000 genomes]
rs17768627	0.83[EUR][1000 genomes]
rs2060910	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2328188	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2328195	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2328198	0.83[EUR][1000 genomes]
rs34559932	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34799456	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35640385	0.82[EUR][1000 genomes]
rs35653218	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35696355	0.84[EUR][1000 genomes]
rs3911274	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4895589	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4896518	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4896529	0.86[EUR][1000 genomes]
rs62429908	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62429909	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62429910	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62430526	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6570439	0.83[EUR][1000 genomes]
rs6922539	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6924491	0.84[EUR][1000 genomes]
rs7754353	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7768881	0.82[EUR][1000 genomes]
rs9389874	0.81[EUR][1000 genomes]
rs9484471	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9484474	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9495910	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9495923	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9495924	0.86[AMR][1000 genomes];0.89[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	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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:141466200-141472600	Weak transcription	Fetal Heart	heart
2	chr6:141466200-141473400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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