Variant report

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

rs_ID	r²[population]
rs10957227	0.91[ASN][1000 genomes]
rs1351364	0.94[ASN][1000 genomes]
rs1351366	0.95[ASN][1000 genomes]
rs1383196	0.95[ASN][1000 genomes]
rs1480186	0.87[ASN][1000 genomes]
rs1531660	0.95[ASN][1000 genomes]
rs1531661	0.95[ASN][1000 genomes]
rs16929130	0.86[ASN][1000 genomes]
rs16929353	0.81[EUR][1000 genomes]
rs16929378	0.81[EUR][1000 genomes]
rs1871592	0.95[ASN][1000 genomes]
rs1993127	0.88[ASN][1000 genomes]
rs1993128	0.84[ASN][1000 genomes]
rs1993129	0.85[ASN][1000 genomes]
rs2199842	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2882924	0.98[ASN][1000 genomes]
rs4366077	0.81[EUR][1000 genomes]
rs4374986	0.95[ASN][1000 genomes]
rs57735770	0.82[EUR][1000 genomes]
rs7826556	0.95[ASN][1000 genomes]
rs7828272	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831339	chr8:63312449-63501127	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv890959	chr8:63449156-63515522	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63490600-63497000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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