Variant report

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

rs_ID	r²[population]
rs1568463	1.00[AMR][1000 genomes]
rs16926482	1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16926510	1.00[AMR][1000 genomes]
rs16926537	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16926544	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16926632	1.00[AMR][1000 genomes]
rs16926652	1.00[AMR][1000 genomes]
rs16926671	1.00[AMR][1000 genomes]
rs16926674	1.00[AMR][1000 genomes]
rs16926677	1.00[AMR][1000 genomes]
rs2051085	1.00[AMR][1000 genomes]
rs2368124	1.00[AMR][1000 genomes]
rs4592324	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59118546	1.00[AMR][1000 genomes]
rs7080297	1.00[AMR][1000 genomes]
rs73610379	1.00[AMR][1000 genomes]
rs7897779	1.00[AMR][1000 genomes]
rs7910941	1.00[AMR][1000 genomes]
rs7924249	1.00[AMR][1000 genomes]
rs8190587	1.00[AMR][1000 genomes]
rs8190623	1.00[AMR][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	esv1792417	chr10:26263695-26395038	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26334200-26342600	Weak transcription	Aorta	Aorta
2	chr10:26337600-26338400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
3	chr10:26338200-26341200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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