Variant report

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

rs_ID	r²[population]
rs10117284	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11140060	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12349789	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13299648	0.84[ASN][1000 genomes]
rs28585601	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3849865	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3860905	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3860906	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3860907	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3860909	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3860912	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3860913	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3860914	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3904187	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3904189	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4297106	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4478644	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4877757	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7019165	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7037795	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7037928	0.86[EUR][1000 genomes];0.84[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	nsv1046491	chr9:85861492-86063992	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85998800-86008600	Weak transcription	Pancreas	Pancrea
2	chr9:86000000-86020600	Weak transcription	Fetal Brain Female	brain
3	chr9:86004600-86014200	Weak transcription	Gastric	stomach
4	chr9:86005400-86021000	Weak transcription	Right Atrium	heart
5	chr9:86007200-86013000	Weak transcription	Fetal Muscle Trunk	muscle
6	chr9:86007400-86012000	Weak transcription	Left Ventricle	heart
7	chr9:86008000-86011600	Weak transcription	HepG2	liver

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