Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1474311	0.86[EUR][1000 genomes]
rs2140325	0.86[EUR][1000 genomes]
rs28842341	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55789229	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55818920	0.86[ASN][1000 genomes]
rs55831634	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55834240	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56036616	0.86[ASN][1000 genomes]
rs56195535	0.95[ASN][1000 genomes]
rs59331691	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60820471	0.83[ASN][1000 genomes]
rs60838705	0.86[ASN][1000 genomes]
rs61447244	0.95[ASN][1000 genomes]
rs61521834	0.86[EUR][1000 genomes]
rs67086694	0.86[ASN][1000 genomes]
rs67150794	0.86[EUR][1000 genomes]
rs68177350	0.95[ASN][1000 genomes]
rs7028869	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7042441	0.86[ASN][1000 genomes]
rs72715609	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72715622	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72715624	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72715625	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72715629	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72715631	0.95[ASN][1000 genomes]
rs72715633	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72715639	0.95[ASN][1000 genomes]
rs72715642	0.95[ASN][1000 genomes]
rs72715648	0.88[ASN][1000 genomes]
rs7849466	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7851933	0.86[ASN][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	nsv613637	chr9:14524438-15011915	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv613647	chr9:14852141-15016475	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv892620	chr9:14922877-15086021	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv892621	chr9:14928013-15043692	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14956200-14958000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr9:14956200-14960800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:14957000-14957400	Enhancers	Placenta	Placenta
4	chr9:14957000-14957600	Enhancers	Fetal Stomach	stomach
5	chr9:14957200-14957400	Enhancers	Adipose Nuclei	Adipose
6	chr9:14957200-14957400	Enhancers	HepG2	liver
7	chr9:14957200-14957600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr9:14957200-14958000	Enhancers	Fetal Muscle Leg	muscle

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