Variant report

Variant	rs4886312
Chromosome Location	chr13:53811878-53811879
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1322948	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1322953	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1322954	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1322960	0.85[EUR][1000 genomes]
rs1407688	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1407689	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1885767	0.84[EUR][1000 genomes]
rs1909650	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1923770	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1923772	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1951724	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1951725	0.84[EUR][1000 genomes]
rs2004422	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2038647	0.86[EUR][1000 genomes]
rs2038648	0.84[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2759674	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2759713	0.85[EUR][1000 genomes]
rs2759714	0.85[EUR][1000 genomes]
rs2806937	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2806940	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2806947	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2806965	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2806968	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2806994	0.81[EUR][1000 genomes]
rs5008125	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7984963	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050969	chr13:53665927-54064861	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr13:53811600-53812200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:53811800-53812600	Enhancers	Cortex derived primary cultured neurospheres	brain

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