Variant report

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

rs_ID	r²[population]
rs11617423	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11619606	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12583021	0.85[EUR][1000 genomes]
rs12583947	0.83[EUR][1000 genomes]
rs12857697	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12873958	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17089405	0.83[EUR][1000 genomes]
rs1932912	0.85[EUR][1000 genomes]
rs34150118	0.84[EUR][1000 genomes]
rs34540611	0.85[EUR][1000 genomes]
rs34751752	0.85[EUR][1000 genomes]
rs4283100	0.83[EUR][1000 genomes]
rs9527199	0.85[EUR][1000 genomes]
rs9527203	0.85[EUR][1000 genomes]
rs9527208	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9536694	0.83[EUR][1000 genomes]
rs9536698	0.83[EUR][1000 genomes]
rs9536699	0.82[EUR][1000 genomes]
rs9536707	0.84[EUR][1000 genomes]
rs9536708	0.84[EUR][1000 genomes]
rs9536709	0.84[EUR][1000 genomes]
rs9536720	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9569024	0.84[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	esv3349795	chr13:54892694-55252030	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr13:54998600-54999000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr13:54998800-55001800	Weak transcription	H9 Cell Line	embryonic stem cell

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