Variant report

Variant	rs66580212
Chromosome Location	chr5:113002078-113002079
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10059373	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10447258	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10478138	0.94[ASN][1000 genomes]
rs11957573	0.83[ASN][1000 genomes]
rs12109672	0.83[ASN][1000 genomes]
rs13170795	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13178544	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs17135859	0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1871910	0.83[ASN][1000 genomes]
rs2016167	0.83[ASN][1000 genomes]
rs2195367	1.00[ASN][1000 genomes]
rs2416323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2416324	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2416325	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2416329	0.94[ASN][1000 genomes]
rs34045110	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34397886	0.83[ASN][1000 genomes]
rs34699212	0.83[ASN][1000 genomes]
rs34783938	0.94[ASN][1000 genomes]
rs34817468	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35039050	0.84[ASN][1000 genomes]
rs35552641	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4329014	0.94[ASN][1000 genomes]
rs4461623	0.89[ASN][1000 genomes]
rs4705467	0.94[ASN][1000 genomes]
rs4705571	0.83[ASN][1000 genomes]
rs4705572	0.83[ASN][1000 genomes]
rs57691496	0.83[ASN][1000 genomes]
rs6881949	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71577455	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7705489	0.83[ASN][1000 genomes]
rs7707681	0.92[AMR][1000 genomes];0.99[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	nsv599407	chr5:112981528-113029914	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	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	chr5:113002000-113007400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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