Variant report

Variant	rs10480716
Chromosome Location	chr7:78874076-78874077
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 106 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10225262	1.00[CEU][hapmap];0.91[JPT][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10230177	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs10234403	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs10235211	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10266537	1.00[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs10270040	1.00[CEU][hapmap]
rs10270764	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs10273845	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10953797	1.00[CEU][hapmap];0.91[CHB][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10953806	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10953812	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10953821	0.86[EUR][1000 genomes]
rs10953825	1.00[CEU][hapmap]
rs10953826	0.85[EUR][1000 genomes]
rs10953827	0.84[EUR][1000 genomes]
rs10953828	0.81[EUR][1000 genomes]
rs10953835	1.00[CEU][hapmap]
rs11532779	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11977493	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12111592	0.84[EUR][1000 genomes]
rs12111980	0.84[EUR][1000 genomes]
rs12154356	1.00[CEU][hapmap];0.83[JPT][hapmap]
rs12154470	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs12216581	1.00[CEU][hapmap]
rs12532467	1.00[CEU][hapmap];0.91[JPT][hapmap]
rs12534590	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12539220	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs12540324	0.85[EUR][1000 genomes]
rs12666243	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs12706101	0.84[EUR][1000 genomes]
rs12706102	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs13222018	0.84[EUR][1000 genomes]
rs13224739	0.86[EUR][1000 genomes]
rs13230579	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs13237396	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13237397	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13240307	0.86[EUR][1000 genomes]
rs13243756	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1358473	1.00[CEU][hapmap];0.83[JPT][hapmap]
rs1406152	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs1406157	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs1406158	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1406159	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1528263	1.00[CEU][hapmap];0.83[JPT][hapmap]
rs1528265	0.80[EUR][1000 genomes]
rs1528269	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs1528270	1.00[CEU][hapmap];0.81[JPT][hapmap]
rs1528271	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1528272	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1528273	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1528274	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1528280	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1528281	0.86[EUR][1000 genomes]
rs1554833	1.00[CEU][hapmap]
rs1554834	1.00[CEU][hapmap]
rs1554835	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs1881292	1.00[CEU][hapmap]
rs1918936	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1918937	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1918938	0.86[EUR][1000 genomes]
rs1918939	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2058393	1.00[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2159709	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2242505	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs2364902	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs28757842	0.85[AMR][1000 genomes]
rs2886212	1.00[CEU][hapmap]
rs34066812	0.86[EUR][1000 genomes]
rs34263368	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4129689	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs4143262	1.00[CEU][hapmap]
rs4256536	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs4445162	0.81[EUR][1000 genomes]
rs4727838	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs4727841	0.81[EUR][1000 genomes]
rs4730746	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs4730747	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs60960798	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6466593	1.00[CEU][hapmap];0.84[JPT][hapmap]
rs6946286	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs6947782	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6950549	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6952164	1.00[CEU][hapmap];0.91[JPT][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6953483	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6953771	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap]
rs6968269	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs71531164	0.86[EUR][1000 genomes]
rs717067	1.00[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7341488	1.00[CEU][hapmap]
rs7455235	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7459140	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs7779953	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap]
rs7781907	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7782460	1.00[CEU][hapmap];0.82[CHB][hapmap];0.87[JPT][hapmap]
rs7782585	1.00[CEU][hapmap];0.91[JPT][hapmap]
rs7805028	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9648980	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs9886146	0.84[EUR][1000 genomes]
rs9886330	0.84[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	nsv464598	chr7:78492642-79483480	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv607659	chr7:78492642-79483480	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1029799	chr7:78608097-79061737	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2757230	chr7:78801388-78887925	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	esv2759539	chr7:78801388-78887925	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv437988	chr7:78806100-78910974	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv831041	chr7:78819499-78973222	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr7:78871200-78875000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:78871400-78875400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:78873200-78874400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr7:78873400-78874600	Enhancers	Brain Hippocampus Middle	brain
5	chr7:78873400-78874800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr7:78873600-78874200	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr7:78873600-78874200	Enhancers	Brain Substantia Nigra	brain
8	chr7:78873600-78874200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr7:78873800-78874200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr7:78873800-78874200	Enhancers	Brain Anterior Caudate	brain
11	chr7:78873800-78874200	Enhancers	Brain Cingulate Gyrus	brain
12	chr7:78873800-78874200	Enhancers	Left Ventricle	heart
13	chr7:78873800-78874200	Enhancers	Ovary	ovary

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