Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:166276597..166279121-chr4:166279967..166282162,2	K562	blood:

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11100606	0.87[ASN][1000 genomes]
rs12498302	0.88[ASN][1000 genomes]
rs12509710	0.88[ASN][1000 genomes]
rs12512757	0.84[ASN][1000 genomes]
rs12641145	0.87[ASN][1000 genomes]
rs13113058	0.88[ASN][1000 genomes]
rs13113441	0.93[ASN][1000 genomes]
rs1438116	0.86[EUR][1000 genomes]
rs1550271	0.82[EUR][1000 genomes]
rs17624714	0.81[ASN][1000 genomes]
rs17686668	0.81[ASN][1000 genomes]
rs1866218	0.83[EUR][1000 genomes]
rs1866219	0.83[EUR][1000 genomes]
rs2322292	0.84[EUR][1000 genomes]
rs35801858	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3775318	0.85[EUR][1000 genomes]
rs4690810	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4691183	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4691184	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59447340	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6827255	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6827346	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6827597	0.87[AMR][1000 genomes]
rs6828152	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs756090	0.84[EUR][1000 genomes]
rs7655392	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7667236	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7690328	0.82[AMR][1000 genomes];0.91[EUR][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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166263200-166280400	Weak transcription	Adipose Nuclei	Adipose
2	chr4:166270000-166276800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:166275400-166277000	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr4:166275600-166277000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr4:166276600-166277200	Weak transcription	Primary B cells from peripheral blood	blood
6	chr4:166276600-166277200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr4:166276600-166277600	Enhancers	HepG2	liver

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