Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10483919	0.88[CEU][hapmap];0.90[EUR][1000 genomes]
rs11849200	0.92[ASN][1000 genomes]
rs150773	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs150775	0.87[CEU][hapmap]
rs154326	0.88[CEU][hapmap]
rs154330	0.89[CEU][hapmap];0.92[EUR][1000 genomes]
rs154337	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs154338	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17108405	0.88[CEU][hapmap];0.91[EUR][1000 genomes]
rs17757946	0.90[EUR][1000 genomes]
rs17757966	0.88[CEU][hapmap];0.90[EUR][1000 genomes]
rs17757972	0.88[CEU][hapmap];0.90[EUR][1000 genomes]
rs17835893	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs17835908	0.88[CEU][hapmap];0.90[EUR][1000 genomes]
rs17835914	0.90[EUR][1000 genomes]
rs220105	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs31444	0.87[CEU][hapmap]
rs31451	0.87[CEU][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs52897	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60536854	0.83[ASN][1000 genomes]
rs61388877	0.94[ASN][1000 genomes]
rs7144101	0.88[JPT][hapmap]
rs7154350	0.86[JPT][hapmap]
rs718787	0.87[CEU][hapmap];0.90[EUR][1000 genomes]
rs74069214	0.97[ASN][1000 genomes]
rs74069237	0.86[ASN][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	nsv832838	chr14:79306627-79445382	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1048274	chr14:79323592-79417906	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv917249	chr14:79388181-79574717	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1041991	chr14:79394408-79644886	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79399000-79400400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:79399000-79400800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:79399600-79399800	Enhancers	HUVEC	blood vessel

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