Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs12494120	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1358238	0.85[ASN][1000 genomes]
rs1405488	0.85[ASN][1000 genomes]
rs1661471	0.85[ASN][1000 genomes]
rs1664131	0.85[ASN][1000 genomes]
rs62295230	0.85[ASN][1000 genomes]
rs62295233	0.85[ASN][1000 genomes]
rs711935	0.85[ASN][1000 genomes]
rs711942	0.83[EUR][1000 genomes]
rs711956	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs711958	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs711961	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73227924	0.93[ASN][1000 genomes]
rs746408	0.92[EUR][1000 genomes]
rs823972	0.85[ASN][1000 genomes]
rs823978	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs824074	0.86[EUR][1000 genomes]
rs824086	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs824088	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824090	0.90[EUR][1000 genomes]
rs824091	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs824093	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs824099	0.94[EUR][1000 genomes]
rs824100	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs844029	0.97[EUR][1000 genomes]
rs850699	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs941132	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9837324	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv460860	chr3:135107678-135769006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv591829	chr3:135107678-135769006	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr3:135131600-135138800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:135134400-135140000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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