Variant report

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

rs_ID	r²[population]
rs10749704	0.82[AMR][1000 genomes]
rs10789017	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10888964	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10888965	0.82[AMR][1000 genomes]
rs11206772	0.82[AFR][1000 genomes]
rs1581994	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs2096086	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2777758	0.81[EUR][1000 genomes]
rs2793663	0.84[EUR][1000 genomes]
rs2793665	0.84[EUR][1000 genomes]
rs2793666	0.84[EUR][1000 genomes]
rs2793672	0.81[EUR][1000 genomes]
rs4550099	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6703556	0.82[AMR][1000 genomes]
rs706362	0.84[AMR][1000 genomes]
rs706371	0.82[AMR][1000 genomes]
rs778395	0.84[AMR][1000 genomes]
rs809018	0.84[AMR][1000 genomes]
rs9436537	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9787032	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9787033	0.92[AFR][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	nsv1006422	chr1:56734772-56828606	Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv534972	chr1:56734772-56828606	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56745400-56757000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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