Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11915601	1.00[EUR][1000 genomes]
rs11927594	1.00[EUR][1000 genomes]
rs13325529	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13327461	1.00[EUR][1000 genomes]
rs28368547	1.00[EUR][1000 genomes]
rs28555456	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4621291	1.00[EUR][1000 genomes]
rs59046488	1.00[EUR][1000 genomes]
rs6762067	1.00[EUR][1000 genomes]
rs6764802	1.00[EUR][1000 genomes]
rs6775388	1.00[EUR][1000 genomes]
rs6786904	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6809595	1.00[EUR][1000 genomes]
rs73014109	1.00[EUR][1000 genomes]
rs73014142	1.00[EUR][1000 genomes]
rs7637292	1.00[EUR][1000 genomes]
rs7648151	1.00[EUR][1000 genomes]
rs9810962	1.00[EUR][1000 genomes]
rs9833026	1.00[EUR][1000 genomes]
rs9844565	1.00[EUR][1000 genomes]
rs9866817	1.00[EUR][1000 genomes]
rs9877749	1.00[EUR][1000 genomes]
rs9882449	1.00[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	nsv592084	chr3:155751484-155830578	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155800200-155811800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:155806800-155808200	Enhancers	Fetal Brain Male	brain

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