Variant report

Variant	rs7795832
Chromosome Location	chr7:79040738-79040739
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs1015639	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs10244234	0.87[EUR][1000 genomes]
rs10254950	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10262441	0.85[EUR][1000 genomes]
rs10272027	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10281359	0.87[EUR][1000 genomes]
rs10452985	0.86[EUR][1000 genomes]
rs10485955	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs10953851	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10953852	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11976606	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11983573	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12672249	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1406165	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs1406166	0.85[EUR][1000 genomes]
rs1528259	0.85[CEU][hapmap];0.84[EUR][1000 genomes]
rs1528260	0.85[CEU][hapmap];0.84[EUR][1000 genomes]
rs1528278	0.87[EUR][1000 genomes]
rs1528279	0.87[EUR][1000 genomes]
rs1528282	0.84[EUR][1000 genomes]
rs16886545	0.84[EUR][1000 genomes]
rs16886548	0.84[EUR][1000 genomes]
rs17152382	0.83[EUR][1000 genomes]
rs17421243	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs1859599	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs1918935	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs2158708	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2190174	0.85[CEU][hapmap];0.84[EUR][1000 genomes]
rs2190175	0.85[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2190179	0.81[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs2364913	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2364918	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28396540	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28459297	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28691838	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34599162	0.87[EUR][1000 genomes]
rs35763479	0.87[EUR][1000 genomes]
rs41364851	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs4141207	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4141208	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4562253	0.83[EUR][1000 genomes]
rs4730806	0.87[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs55637636	0.87[EUR][1000 genomes]
rs55713683	0.87[EUR][1000 genomes]
rs58310347	0.87[EUR][1000 genomes]
rs6466621	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs66499867	0.87[EUR][1000 genomes]
rs66775453	0.87[EUR][1000 genomes]
rs66778115	0.87[EUR][1000 genomes]
rs66900251	0.87[EUR][1000 genomes]
rs66961385	0.87[EUR][1000 genomes]
rs67092648	0.87[EUR][1000 genomes]
rs67122557	0.87[EUR][1000 genomes]
rs67289031	0.87[EUR][1000 genomes]
rs67486505	0.87[EUR][1000 genomes]
rs67685126	0.85[EUR][1000 genomes]
rs68113978	0.87[EUR][1000 genomes]
rs6946286	0.82[JPT][hapmap]
rs6947186	0.87[EUR][1000 genomes]
rs6964030	0.86[EUR][1000 genomes]
rs6964349	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs6966753	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs727391	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73141612	0.87[EUR][1000 genomes]
rs73156041	0.84[EUR][1000 genomes]
rs73156043	0.84[EUR][1000 genomes]
rs73156068	0.83[EUR][1000 genomes]
rs73156084	0.84[EUR][1000 genomes]
rs73157803	0.87[EUR][1000 genomes]
rs73157805	0.87[EUR][1000 genomes]
rs73157824	0.87[EUR][1000 genomes]
rs73157844	0.87[EUR][1000 genomes]
rs73157878	0.87[EUR][1000 genomes]
rs73381312	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7455557	0.86[EUR][1000 genomes]
rs7778707	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs7785706	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7788509	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7792796	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7799230	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7803773	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7806210	0.84[EUR][1000 genomes]
rs7807048	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7808561	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs970491	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs984708	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs991259	0.87[CHB][hapmap];0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs9918566	0.87[EUR][1000 genomes]
rs993860	0.96[CHB][hapmap];0.91[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9969308	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9969320	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 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	esv2764028	chr7:78874740-79112630	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv888514	chr7:78987060-79061837	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv888515	chr7:78987060-79221707	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv607664	chr7:78998409-79057761	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv607665	chr7:79027730-79063644	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv607666	chr7:79029872-79063644	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv607667	chr7:79029872-79065268	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv607668	chr7:79029872-79070452	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv427792	chr7:79039802-79253373	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79031000-79040800	Weak transcription	Brain Anterior Caudate	brain
2	chr7:79036800-79044200	Weak transcription	Adipose Nuclei	Adipose
3	chr7:79037200-79048800	Weak transcription	NHLF	lung
4	chr7:79037400-79040800	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr7:79037400-79041600	Weak transcription	Brain Angular Gyrus	brain
6	chr7:79037400-79041600	Weak transcription	Brain Cingulate Gyrus	brain
7	chr7:79039600-79041200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr7:79040000-79043800	Weak transcription	NHDF-Ad	bronchial
9	chr7:79040000-79048800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr7:79040000-79049200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:79040200-79041600	Enhancers	Brain Hippocampus Middle	brain
12	chr7:79040600-79042200	Enhancers	Brain Substantia Nigra	brain

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