Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs2790937	0.94[ASN][1000 genomes]
rs2790938	0.97[ASN][1000 genomes]
rs2790939	0.83[ASN][1000 genomes]
rs2790941	0.97[ASN][1000 genomes]
rs2790942	0.97[ASN][1000 genomes]
rs2790944	0.97[ASN][1000 genomes]
rs2790946	0.97[ASN][1000 genomes]
rs709625	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72792210	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72792211	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs755120	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs786779	1.00[ASN][1000 genomes]
rs786780	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786783	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786784	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786785	0.83[ASN][1000 genomes]
rs786787	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786793	0.93[ASN][1000 genomes]
rs786806	0.97[ASN][1000 genomes]
rs786808	0.97[ASN][1000 genomes]
rs786822	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs813092	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[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	esv2758218	chr10:48593396-49299273	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	esv2759748	chr10:48593396-49299273	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:48657600-48663800	Enhancers	Fetal Lung	lung
2	chr10:48658400-48661800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:48658600-48658800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
4	chr10:48658600-48660600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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