Variant report

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

rs_ID	r²[population]
rs10015366	0.87[ASW][hapmap];0.83[MKK][hapmap]
rs12507012	0.95[ASN][1000 genomes]
rs13105212	0.85[JPT][hapmap]
rs1442099	0.85[JPT][hapmap]
rs1442101	0.85[JPT][hapmap]
rs3906823	0.85[JPT][hapmap]
rs4315750	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4374601	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4396968	0.83[JPT][hapmap]
rs4501194	0.85[JPT][hapmap]
rs4521322	0.84[ASN][1000 genomes]
rs4597805	0.87[ASW][hapmap];0.92[JPT][hapmap];0.93[TSI][hapmap];0.88[ASN][1000 genomes]
rs6447534	0.85[JPT][hapmap]
rs6829206	0.83[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6837255	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6846701	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7666212	0.85[JPT][hapmap]
rs7680321	0.85[JPT][hapmap]
rs7680746	0.85[JPT][hapmap]
rs9291304	0.83[JPT][hapmap]
rs993776	0.91[JPT][hapmap]

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	esv3395099	chr4:47043545-47045643	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47036200-47050200	Weak transcription	Brain Anterior Caudate	brain

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