Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11100606	0.83[ASN][1000 genomes]
rs11732637	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12498302	0.83[ASN][1000 genomes]
rs12509710	0.84[ASN][1000 genomes]
rs12512757	0.87[ASN][1000 genomes]
rs12641145	0.83[ASN][1000 genomes]
rs13113058	0.83[ASN][1000 genomes]
rs13113441	0.88[ASN][1000 genomes]
rs1438116	0.87[EUR][1000 genomes]
rs1550271	0.84[EUR][1000 genomes]
rs1866218	0.84[EUR][1000 genomes]
rs1866219	0.84[EUR][1000 genomes]
rs2322292	0.85[EUR][1000 genomes]
rs3775318	0.86[EUR][1000 genomes]
rs4690810	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4691183	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4691184	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59447340	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6827255	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6827346	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6827597	0.83[AMR][1000 genomes]
rs6828152	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs756090	0.85[EUR][1000 genomes]
rs7655392	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7667236	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7690328	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1847399	chr4:166259587-166284836	Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
2	esv2763404	chr4:166265940-166275340	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166263200-166280400	Weak transcription	Adipose Nuclei	Adipose
2	chr4:166264200-166274800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr4:166270000-166276800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:166273200-166276600	Weak transcription	HepG2	liver
5	chr4:166274600-166275600	Enhancers	Primary monocytes fromperipheralblood	blood

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