Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs13108711	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13111601	0.82[CEU][hapmap];0.82[EUR][1000 genomes]
rs13117081	0.82[EUR][1000 genomes]
rs13133420	1.00[CEU][hapmap]
rs13136231	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13143186	0.82[EUR][1000 genomes]
rs13143690	0.82[EUR][1000 genomes]
rs34267891	0.82[EUR][1000 genomes]
rs34455147	0.82[EUR][1000 genomes]
rs34533457	0.82[EUR][1000 genomes]
rs34746571	0.82[EUR][1000 genomes]
rs35131545	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35649307	0.82[EUR][1000 genomes]
rs61201051	0.82[EUR][1000 genomes]
rs61792942	0.82[EUR][1000 genomes]
rs61792944	0.82[EUR][1000 genomes]
rs61792946	0.82[EUR][1000 genomes]
rs61792947	0.82[EUR][1000 genomes]
rs71598138	0.82[EUR][1000 genomes]
rs7696734	0.82[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv878811	chr4:30987395-31019279	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30998000-31018000	Weak transcription	Aorta	Aorta

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