Variant report

Variant	rs4145084
Chromosome Location	chr10:90235902-90235903
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10509551	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10887822	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10887830	1.00[ASN][1000 genomes]
rs10887831	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs11202746	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11202748	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11202752	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11202754	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11202757	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11202761	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11202766	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12357364	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12357948	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12359950	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12360281	0.89[AMR][1000 genomes]
rs12413139	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12413825	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12572235	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1325906	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1342455	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1342458	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1536252	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17112571	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17112575	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1891431	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2153855	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2185785	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2437877	0.81[AFR][1000 genomes]
rs28794023	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2986118	0.81[AFR][1000 genomes]
rs4520503	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4933482	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4933483	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4934406	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4934407	0.87[ASN][1000 genomes]
rs4934410	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61640455	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7076491	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73355485	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73355487	0.86[AMR][1000 genomes]
rs9664569	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482385	chr10:90066140-90259751	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv948664	chr10:90076715-90517150	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1054984	chr10:90122512-90278038	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1050587	chr10:90146582-90272627	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv540739	chr10:90146582-90272627	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv529324	chr10:90198865-90738588	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv825500	chr10:90221443-90302503	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	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	chr10:90227600-90237000	Weak transcription	Left Ventricle	heart
2	chr10:90233000-90236000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:90233800-90239200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr10:90234200-90236000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr10:90234400-90238200	Weak transcription	Right Ventricle	heart
6	chr10:90235000-90236000	Enhancers	HMEC	breast
7	chr10:90235000-90237000	Weak transcription	Psoas Muscle	Psoas
8	chr10:90235000-90240400	Weak transcription	Aorta	Aorta
9	chr10:90235200-90237000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr10:90235200-90237200	Weak transcription	NHEK	skin
11	chr10:90235400-90237400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr10:90235400-90237800	Weak transcription	Fetal Heart	heart
13	chr10:90235400-90238200	Weak transcription	HSMM	muscle
14	chr10:90235600-90236400	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr10:90235600-90237200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr10:90235600-90238600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr10:90235600-90238800	Weak transcription	Ovary	ovary

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