Variant report

Variant	rs4275306
Chromosome Location	chr9:15095216-15095217
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10116796	1.00[AFR][1000 genomes]
rs10120028	1.00[AFR][1000 genomes]
rs10121250	1.00[AFR][1000 genomes]
rs10122944	1.00[AFR][1000 genomes]
rs10756646	0.94[AFR][1000 genomes]
rs10810345	0.87[AFR][1000 genomes]
rs10810346	1.00[AFR][1000 genomes]
rs1746330	0.84[AFR][1000 genomes]
rs1780161	0.84[AFR][1000 genomes]
rs1936713	1.00[AFR][1000 genomes]
rs1936714	1.00[AFR][1000 genomes]
rs1936720	1.00[AFR][1000 genomes]
rs1936721	1.00[AFR][1000 genomes]
rs2105414	1.00[AFR][1000 genomes]
rs2105415	1.00[AFR][1000 genomes]
rs2186027	1.00[YRI][hapmap]
rs2382516	1.00[AFR][1000 genomes]
rs2761092	0.87[AFR][1000 genomes]
rs2761103	0.87[AFR][1000 genomes]
rs2761110	0.81[AFR][1000 genomes]
rs2761111	0.81[AFR][1000 genomes]
rs2761114	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs2761117	0.91[AFR][1000 genomes]
rs2800569	0.81[AFR][1000 genomes]
rs2800592	1.00[YRI][hapmap]
rs2800597	0.87[AFR][1000 genomes]
rs2800614	0.84[AFR][1000 genomes]
rs2800616	0.84[AFR][1000 genomes]
rs2800619	0.84[AFR][1000 genomes]
rs2800620	0.84[AFR][1000 genomes]
rs4237137	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs4269631	0.91[AFR][1000 genomes]
rs4305996	0.91[AFR][1000 genomes]
rs4307425	1.00[AFR][1000 genomes]
rs4373617	1.00[AFR][1000 genomes]
rs4401969	1.00[AFR][1000 genomes]
rs4451417	1.00[AFR][1000 genomes]
rs4517211	1.00[AFR][1000 genomes]
rs4520265	0.94[AFR][1000 genomes]
rs4526461	1.00[AFR][1000 genomes]
rs4559332	0.97[AFR][1000 genomes]
rs4579616	1.00[AFR][1000 genomes]
rs4740601	1.00[AFR][1000 genomes]
rs4740602	0.91[AFR][1000 genomes]
rs4741456	0.94[AFR][1000 genomes]
rs4741457	1.00[AFR][1000 genomes]
rs4741458	0.94[AFR][1000 genomes]
rs4741459	1.00[AFR][1000 genomes]
rs4741460	0.91[AFR][1000 genomes]
rs4741461	1.00[AFR][1000 genomes]
rs486612	0.87[YRI][hapmap]
rs613899	0.87[YRI][hapmap]
rs616584	0.87[YRI][hapmap]
rs6474891	1.00[AFR][1000 genomes]
rs6474892	1.00[AFR][1000 genomes]
rs6474894	0.94[AFR][1000 genomes]
rs7019779	1.00[AFR][1000 genomes]
rs7019934	0.90[AFR][1000 genomes]
rs7466658	1.00[AFR][1000 genomes]
rs7466688	1.00[AFR][1000 genomes]
rs7469171	1.00[AFR][1000 genomes]
rs7469190	1.00[AFR][1000 genomes]
rs9298721	1.00[AFR][1000 genomes]
rs9298722	1.00[AFR][1000 genomes]
rs9298723	1.00[AFR][1000 genomes]
rs9298724	1.00[AFR][1000 genomes]
rs9987459	1.00[AFR][1000 genomes]
rs9987584	1.00[AFR][1000 genomes]
rs9987587	1.00[AFR][1000 genomes]
rs9987728	0.88[AFR][1000 genomes]
rs9987732	1.00[AFR][1000 genomes]
rs9987917	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831519	chr9:15018160-15209127	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1019567	chr9:15031398-15159409	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv892623	chr9:15079847-15127129	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	esv3432932	chr9:15095054-15095288	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15088200-15096800	Weak transcription	Fetal Lung	lung

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