Variant report

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

rs_ID	r²[population]
rs11618690	0.90[ASN][1000 genomes]
rs11618708	0.90[ASN][1000 genomes]
rs17571410	0.87[ASN][1000 genomes]
rs17571928	0.96[ASN][1000 genomes]
rs17650122	0.91[ASN][1000 genomes]
rs186586	0.94[ASN][1000 genomes]
rs2475538	0.96[ASN][1000 genomes]
rs2479757	0.96[ASN][1000 genomes]
rs2479758	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2987336	0.95[ASN][1000 genomes]
rs3011022	1.00[ASN][1000 genomes]
rs326507	0.98[ASN][1000 genomes]
rs326508	0.96[ASN][1000 genomes]
rs326520	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4377014	1.00[ASN][1000 genomes]
rs4769659	0.90[ASN][1000 genomes]
rs56023620	0.91[ASN][1000 genomes]
rs59155661	0.91[ASN][1000 genomes]
rs61946436	0.81[ASN][1000 genomes]
rs621417	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7329021	0.91[ASN][1000 genomes]
rs7986484	0.90[ASN][1000 genomes]
rs7992303	0.96[ASN][1000 genomes]
rs7994188	0.91[ASN][1000 genomes]
rs7999249	0.91[ASN][1000 genomes]
rs7999783	0.89[ASN][1000 genomes]
rs8000492	0.90[ASN][1000 genomes]
rs8001303	0.88[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	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 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	chr13:29606200-29623600	Weak transcription	Aorta	Aorta
2	chr13:29609400-29613200	Weak transcription	Fetal Heart	heart

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