Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12718290	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13221147	1.00[CHD][hapmap]
rs13223000	0.86[CEU][hapmap];0.84[EUR][1000 genomes]
rs13224880	1.00[CHD][hapmap]
rs13228431	1.00[CHD][hapmap]
rs13230347	1.00[CHD][hapmap];0.83[GIH][hapmap]
rs13234438	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13234500	0.87[CEU][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13237182	1.00[CHD][hapmap]
rs13244837	0.84[AMR][1000 genomes]
rs1527836	1.00[CHD][hapmap]
rs17132435	1.00[CHD][hapmap]
rs17132489	1.00[CHD][hapmap]
rs34021932	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34598210	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35302464	0.84[EUR][1000 genomes]
rs35316325	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35483521	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62447337	0.80[EUR][1000 genomes]
rs62447353	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62447359	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62448770	0.94[AMR][1000 genomes]
rs6583453	1.00[CHD][hapmap]
rs6946184	0.83[GIH][hapmap]
rs7785482	1.00[CHD][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	nsv606894	chr7:48663637-48718598	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48672600-48688800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:48683400-48689000	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr7:48685600-48687200	Weak transcription	Fetal Heart	heart
4	chr7:48686200-48687200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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