Variant report

Variant	rs7678386
Chromosome Location	chr4:30891187-30891188
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10000401	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10013694	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10805300	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10939317	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10939318	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11722640	0.81[EUR][1000 genomes]
rs11727594	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11735048	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12512796	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13120686	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13127450	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13151051	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28670870	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2871476	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4075130	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4235012	0.90[ASN][1000 genomes]
rs4235013	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4235014	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4235015	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4259023	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4260492	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4261943	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4266255	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4337695	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4358358	0.81[EUR][1000 genomes]
rs4374588	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4380481	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4469028	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4487300	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4491979	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4536889	0.80[EUR][1000 genomes]
rs4557225	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4585258	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4692107	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4692487	0.80[EUR][1000 genomes]
rs4692488	0.80[EUR][1000 genomes]
rs4692490	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5001866	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6448726	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6448727	0.80[EUR][1000 genomes]
rs6819406	0.81[EUR][1000 genomes]
rs6839087	0.81[EUR][1000 genomes]
rs6840698	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7658077	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7661924	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7662881	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7669015	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7673048	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7683848	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7683968	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7696462	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9685207	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9990832	0.80[EUR][1000 genomes]
rs9997529	0.80[EUR][1000 genomes]
rs9999771	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]

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	nsv878810	chr4:30823157-30987395	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	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

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30870800-30903200	Weak transcription	Fetal Lung	lung
2	chr4:30879800-30893000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:30883200-30899000	Weak transcription	Aorta	Aorta

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