Variant report

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

rs_ID	r²[population]
rs1495370	0.94[ASN][1000 genomes]
rs17055973	0.94[ASN][1000 genomes]
rs17055980	0.94[ASN][1000 genomes]
rs17056024	0.82[ASN][1000 genomes]
rs56357131	0.82[ASN][1000 genomes]
rs59686659	0.82[ASN][1000 genomes]
rs61500900	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62249344	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62249347	0.94[ASN][1000 genomes]
rs62249348	0.94[ASN][1000 genomes]
rs62249349	0.82[ASN][1000 genomes]
rs62249353	0.82[ASN][1000 genomes]
rs62251577	0.82[ASN][1000 genomes]
rs66539449	0.82[ASN][1000 genomes]
rs72877115	0.82[ASN][1000 genomes]
rs7609626	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7617166	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7636943	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9819181	0.89[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9820522	0.82[ASN][1000 genomes]
rs9840584	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[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	nsv876814	chr3:55802749-55860526	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island 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	chr3:55801800-55804000	Weak transcription	Pancreas	Pancrea

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