Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1000458	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1000459	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10164668	0.80[AMR][1000 genomes]
rs10196032	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10432645	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12998704	0.81[EUR][1000 genomes]
rs1405342	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1526616	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1526618	0.83[AMR][1000 genomes]
rs1526631	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1589948	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1609006	0.85[AMR][1000 genomes]
rs1609007	0.86[AMR][1000 genomes]
rs1852365	0.91[AMR][1000 genomes]
rs1949924	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2860733	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4853212	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4853214	0.82[AFR][1000 genomes]
rs6704909	0.82[ASN][1000 genomes]
rs6747714	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6747727	0.81[ASN][1000 genomes]
rs6748106	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6760707	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7567752	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7574697	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[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	esv3362472	chr2:76524237-76524459	Weak transcription	n/a	n/a	inside rSNPs	diseases
2	nsv1006097	chr2:76524248-76675427	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	1 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	chr2:76520600-76524800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:76522800-76525400	Weak transcription	Fetal Heart	heart
3	chr2:76523800-76524600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr2:76523800-76525200	Weak transcription	Fetal Lung	lung

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