Variant report

Variant	rs58349179
Chromosome Location	chr5:127965440-127965441
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 124 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:120)

rs_ID	r²[population]
rs10428533	1.00[ASN][1000 genomes]
rs10428593	1.00[ASN][1000 genomes]
rs11951267	0.91[EUR][1000 genomes]
rs11955937	0.91[EUR][1000 genomes]
rs12109254	0.89[ASN][1000 genomes]
rs13154414	1.00[ASN][1000 genomes]
rs13158744	1.00[ASN][1000 genomes]
rs13162214	1.00[ASN][1000 genomes]
rs13168624	1.00[ASN][1000 genomes]
rs13172385	1.00[ASN][1000 genomes]
rs13179269	1.00[ASN][1000 genomes]
rs13181957	1.00[ASN][1000 genomes]
rs13186444	1.00[ASN][1000 genomes]
rs1363468	1.00[ASN][1000 genomes]
rs1363469	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17164083	0.80[EUR][1000 genomes]
rs17164086	0.80[EUR][1000 genomes]
rs17615636	0.80[EUR][1000 genomes]
rs34912177	1.00[ASN][1000 genomes]
rs34968180	1.00[ASN][1000 genomes]
rs35024105	1.00[ASN][1000 genomes]
rs35454462	1.00[ASN][1000 genomes]
rs4305681	1.00[ASN][1000 genomes]
rs4377749	1.00[ASN][1000 genomes]
rs4380709	0.91[EUR][1000 genomes]
rs4386769	0.90[EUR][1000 genomes]
rs4400171	0.91[EUR][1000 genomes]
rs4410683	0.88[EUR][1000 genomes]
rs4418144	1.00[ASN][1000 genomes]
rs4425555	0.91[EUR][1000 genomes]
rs4425556	0.91[EUR][1000 genomes]
rs4493716	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4496752	0.91[EUR][1000 genomes]
rs4521535	1.00[ASN][1000 genomes]
rs4557470	0.88[EUR][1000 genomes]
rs4577751	0.91[EUR][1000 genomes]
rs4580821	0.91[EUR][1000 genomes]
rs4587123	1.00[ASN][1000 genomes]
rs4620068	0.91[EUR][1000 genomes]
rs55683423	0.91[EUR][1000 genomes]
rs55696017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55791343	0.88[EUR][1000 genomes]
rs55840580	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56018106	0.88[EUR][1000 genomes]
rs56173634	0.91[EUR][1000 genomes]
rs56232757	0.91[EUR][1000 genomes]
rs56358260	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56766733	0.91[EUR][1000 genomes]
rs57454105	0.91[EUR][1000 genomes]
rs59143127	0.91[EUR][1000 genomes]
rs59567527	0.90[EUR][1000 genomes]
rs60574263	0.91[EUR][1000 genomes]
rs61081409	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61358597	0.86[EUR][1000 genomes]
rs61375240	0.91[EUR][1000 genomes]
rs6595840	0.91[EUR][1000 genomes]
rs67031953	1.00[ASN][1000 genomes]
rs6863062	0.91[EUR][1000 genomes]
rs6863262	0.91[EUR][1000 genomes]
rs6863380	0.91[EUR][1000 genomes]
rs6863460	0.91[EUR][1000 genomes]
rs6865828	0.80[EUR][1000 genomes]
rs6870746	0.90[EUR][1000 genomes]
rs6876609	0.91[EUR][1000 genomes]
rs6880762	0.91[EUR][1000 genomes]
rs6886451	0.88[EUR][1000 genomes]
rs6891153	0.91[EUR][1000 genomes]
rs6891166	0.91[EUR][1000 genomes]
rs71587985	0.89[ASN][1000 genomes]
rs73346354	0.80[EUR][1000 genomes]
rs73348066	0.90[EUR][1000 genomes]
rs73348070	0.91[EUR][1000 genomes]
rs73348077	0.91[EUR][1000 genomes]
rs73348078	0.88[EUR][1000 genomes]
rs73348080	0.91[EUR][1000 genomes]
rs73348085	0.91[EUR][1000 genomes]
rs73348087	0.91[EUR][1000 genomes]
rs73348099	0.91[EUR][1000 genomes]
rs73348102	0.91[EUR][1000 genomes]
rs73348278	0.80[EUR][1000 genomes]
rs73348280	0.80[EUR][1000 genomes]
rs73348287	0.80[EUR][1000 genomes]
rs73348296	0.88[EUR][1000 genomes]
rs73348299	0.91[EUR][1000 genomes]
rs73350104	0.91[EUR][1000 genomes]
rs73350106	0.91[EUR][1000 genomes]
rs73350109	0.91[EUR][1000 genomes]
rs73350115	0.91[EUR][1000 genomes]
rs73350129	0.91[EUR][1000 genomes]
rs73350134	0.88[EUR][1000 genomes]
rs73350195	0.91[EUR][1000 genomes]
rs73351861	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73351865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73351884	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73352205	0.91[EUR][1000 genomes]
rs73352207	0.91[EUR][1000 genomes]
rs73352225	0.91[EUR][1000 genomes]
rs73352737	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73352741	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73352743	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7447218	0.91[EUR][1000 genomes]
rs7700287	0.91[EUR][1000 genomes]
rs7704921	0.91[EUR][1000 genomes]
rs7709202	0.91[EUR][1000 genomes]
rs7709476	0.90[EUR][1000 genomes]
rs7709634	0.91[EUR][1000 genomes]
rs7714023	0.91[EUR][1000 genomes]
rs7714465	0.91[EUR][1000 genomes]
rs7714623	0.90[EUR][1000 genomes]
rs7715766	1.00[ASN][1000 genomes]
rs7720190	0.91[EUR][1000 genomes]
rs7724233	0.90[EUR][1000 genomes]
rs7724383	0.90[EUR][1000 genomes]
rs7728360	1.00[ASN][1000 genomes]
rs7728409	0.91[EUR][1000 genomes]
rs7730875	0.91[EUR][1000 genomes]
rs7732171	0.91[EUR][1000 genomes]
rs7734405	0.91[EUR][1000 genomes]
rs7734534	0.91[EUR][1000 genomes]
rs7735831	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531991	chr5:127624564-127966085	Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv427734	chr5:127805281-128088632	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830484	chr5:127936347-128087308	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1023405	chr5:127955360-128190069	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs58349179	FBN2	cis	Whole Blood	GTEx
rs58349179	FBN2	cis	Nerve Tibial	GTEx
rs58349179	FBN2	cis	Artery Tibial	GTEx
rs58349179	FBN2	cis	Artery Aorta	GTEx
rs58349179	FBN2	cis	Adipose Subcutaneous	GTEx
rs58349179	FBN2	cis	lung	GTEx
rs58349179	FBN2	cis	Thyroid	GTEx

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:127964400-127965600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:127964400-127966200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr5:127964600-127965600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:127964600-127965600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr5:127964800-127965600	Enhancers	Fetal Heart	heart
6	chr5:127965000-127966000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr5:127965000-127966200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:127965000-127966400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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