Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10499601	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11509900	0.86[EUR][1000 genomes]
rs12114004	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12154511	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1524051	0.82[EUR][1000 genomes]
rs1524052	0.82[EUR][1000 genomes]
rs17171277	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1949774	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2140532	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2392527	0.82[EUR][1000 genomes]
rs4430011	0.82[EUR][1000 genomes]
rs61618798	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs73691906	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs73691948	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73691971	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73691975	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs952368	0.82[EUR][1000 genomes]
rs952369	0.82[EUR][1000 genomes]
rs9648058	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9648458	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9648459	0.87[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	nsv8074	chr7:37865340-38210087	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv887962	chr7:38093233-38203341	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38141400-38142000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:38141600-38141800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:38141600-38142200	Enhancers	HSMMtube	muscle
4	chr7:38141600-38142400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:38141600-38143000	Enhancers	Primary hematopoietic stem cells	blood

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