Variant report

Variant	rs73303052
Chromosome Location	chr7:3567389-3567390
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs12114017	1.00[AMR][1000 genomes]
rs28396741	1.00[AMR][1000 genomes]
rs56945505	1.00[AMR][1000 genomes]
rs57519297	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60368813	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73293132	1.00[AMR][1000 genomes]
rs73293152	1.00[AMR][1000 genomes]
rs73293175	1.00[AMR][1000 genomes]
rs73293185	1.00[AMR][1000 genomes]
rs73296236	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73296244	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73296252	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73296254	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73296260	1.00[AMR][1000 genomes]
rs73296264	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73296269	1.00[AFR][1000 genomes]
rs73296271	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73296276	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73296288	1.00[AMR][1000 genomes]
rs73296291	1.00[AMR][1000 genomes]
rs73296295	1.00[AMR][1000 genomes]
rs73296301	1.00[AMR][1000 genomes]
rs73296760	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73296766	1.00[AMR][1000 genomes]
rs73298214	1.00[AMR][1000 genomes]
rs73298216	1.00[AMR][1000 genomes]
rs73298217	1.00[AMR][1000 genomes]
rs73298227	1.00[AMR][1000 genomes]
rs73298232	1.00[AMR][1000 genomes]
rs73298246	1.00[AMR][1000 genomes]
rs73298370	1.00[AMR][1000 genomes]
rs73298373	1.00[AMR][1000 genomes]
rs73298374	1.00[AMR][1000 genomes]
rs73298379	1.00[AMR][1000 genomes]
rs73298387	1.00[AMR][1000 genomes]
rs73298397	1.00[AMR][1000 genomes]
rs73300393	1.00[AMR][1000 genomes]
rs73300394	1.00[AMR][1000 genomes]
rs73302308	1.00[AMR][1000 genomes]
rs73302316	1.00[AMR][1000 genomes]
rs73302318	1.00[AMR][1000 genomes]
rs73303045	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303062	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303065	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303071	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73309905	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73309923	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73309930	1.00[AMR][1000 genomes]
rs7789842	1.00[AMR][1000 genomes]
rs7804193	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018173	chr7:3258989-3879848	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv538660	chr7:3258989-3879848	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1016555	chr7:3298478-3872512	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv538661	chr7:3298478-3872512	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2764026	chr7:3365002-3618361	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv916071	chr7:3423207-3697428	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv528715	chr7:3451251-3598581	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv605902	chr7:3464896-3598581	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv464270	chr7:3490865-3581357	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv605904	chr7:3490865-3581357	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1034716	chr7:3512406-3616155	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv887334	chr7:3531275-3635105	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv1023888	chr7:3539750-3638242	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv1034298	chr7:3539750-3646251	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv1030363	chr7:3541046-3577665	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv1029264	chr7:3549193-3622532	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv1032031	chr7:3554760-3609584	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv538675	chr7:3554760-3609584	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv464271	chr7:3556132-3605340	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv605905	chr7:3556132-3605340	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv1025623	chr7:3558521-3606640	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv605906	chr7:3559826-3605340	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv1027274	chr7:3561252-3602457	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv538676	chr7:3561252-3602457	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
25	nsv1034671	chr7:3565156-3607294	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
26	nsv538677	chr7:3565156-3607294	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
27	nsv1028274	chr7:3565356-3607155	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
28	nsv538678	chr7:3565356-3607155	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3549400-3577000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:3564600-3567400	Enhancers	Fetal Brain Male	brain
3	chr7:3565200-3568000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:3567000-3567400	Weak transcription	Spleen	Spleen
5	chr7:3567000-3567600	Enhancers	Gastric	stomach
6	chr7:3567000-3567600	Enhancers	Pancreas	Pancrea
7	chr7:3567200-3567400	Enhancers	Right Ventricle	heart
8	chr7:3567200-3569200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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