Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs12101515	1.00[EUR][1000 genomes]
rs12102022	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12102026	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1589315	1.00[EUR][1000 genomes]
rs28369578	1.00[EUR][1000 genomes]
rs28414510	1.00[EUR][1000 genomes]
rs28440101	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28489023	0.81[AFR][1000 genomes]
rs28502057	1.00[EUR][1000 genomes]
rs28533229	1.00[EUR][1000 genomes]
rs28585621	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28649518	1.00[EUR][1000 genomes]
rs28650843	1.00[EUR][1000 genomes]
rs28662932	1.00[EUR][1000 genomes]
rs28837800	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28866807	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs497723	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs501022	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs517562	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs547426	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs569024	1.00[YRI][hapmap]
rs572886	1.00[YRI][hapmap]
rs573320	1.00[YRI][hapmap]
rs580558	0.83[YRI][hapmap]
rs7167636	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7170707	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8024574	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8038891	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8042489	0.84[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv1845471	chr15:54556063-54685463	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54679800-54680800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr15:54680200-54690200	Weak transcription	Aorta	Aorta

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