Variant report

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10764597	0.81[ASN][1000 genomes]
rs10828940	0.88[ASN][1000 genomes]
rs10828942	0.87[ASN][1000 genomes]
rs10828943	0.87[ASN][1000 genomes]
rs10828947	0.86[ASN][1000 genomes]
rs10828948	0.82[ASN][1000 genomes]
rs11014913	0.83[ASN][1000 genomes]
rs11014937	0.86[ASN][1000 genomes]
rs12779127	0.89[ASN][1000 genomes]
rs1339817	0.83[ASN][1000 genomes]
rs1416859	0.88[ASN][1000 genomes]
rs1416863	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1578217	0.89[ASN][1000 genomes]
rs1851146	0.80[ASN][1000 genomes]
rs1915477	0.87[ASN][1000 genomes]
rs1976828	0.89[ASN][1000 genomes]
rs2027356	0.81[ASN][1000 genomes]
rs2204023	0.81[ASN][1000 genomes]
rs2368118	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2368121	0.84[ASN][1000 genomes]
rs2947353	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3006270	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs3737275	0.81[ASN][1000 genomes]
rs3824699	0.86[ASN][1000 genomes]
rs4403709	0.86[ASN][1000 genomes]
rs4747545	0.85[ASN][1000 genomes]
rs7077072	0.88[ASN][1000 genomes]
rs7084614	0.86[ASN][1000 genomes]
rs7100134	0.83[ASN][1000 genomes]
rs7905199	0.81[ASN][1000 genomes]
rs7914361	0.81[ASN][1000 genomes]
rs982082	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs993397	0.81[ASN][1000 genomes]
rs993398	0.81[ASN][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	chr10:26327600-26336800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr10:26334200-26342600	Weak transcription	Aorta	Aorta
3	chr10:26335200-26335800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet

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