Variant report

Variant	rs73327195
Chromosome Location	chr14:78878575-78878576
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs17107424	0.81[ASN][1000 genomes]
rs17107444	0.81[ASN][1000 genomes]
rs17107516	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17107519	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17107523	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17107530	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17107594	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs17107611	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs56923572	1.00[AMR][1000 genomes]
rs58330928	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs59762056	1.00[AMR][1000 genomes]
rs59819728	1.00[AMR][1000 genomes]
rs61052532	1.00[AMR][1000 genomes]
rs61199699	0.81[ASN][1000 genomes]
rs73308947	0.81[ASN][1000 genomes]
rs73308971	0.81[ASN][1000 genomes]
rs73308985	0.81[ASN][1000 genomes]
rs73309000	0.81[ASN][1000 genomes]
rs73310817	0.81[ASN][1000 genomes]
rs73310826	0.81[ASN][1000 genomes]
rs73316006	0.94[ASN][1000 genomes]
rs73316040	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73316042	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73316045	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73316421	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316436	1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs73316456	1.00[AMR][1000 genomes]
rs73316459	1.00[AMR][1000 genomes]
rs73316471	1.00[AMR][1000 genomes]
rs73316478	1.00[AMR][1000 genomes]
rs73319533	0.81[ASN][1000 genomes]
rs73319535	0.81[ASN][1000 genomes]
rs73319540	0.81[ASN][1000 genomes]
rs73320490	1.00[AMR][1000 genomes]
rs73320491	1.00[AMR][1000 genomes]
rs73324490	1.00[AMR][1000 genomes]
rs73327200	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73329110	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73329120	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73329172	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs8015539	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832837	chr14:78766805-78946526	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	esv2757577	chr14:78875607-78912967	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv2760000	chr14:78875607-79173528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78873400-78880600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr14:78873400-78881400	Weak transcription	Brain Anterior Caudate	brain
3	chr14:78873600-78880600	Weak transcription	Brain Angular Gyrus	brain
4	chr14:78874200-78881000	Weak transcription	Brain Hippocampus Middle	brain
5	chr14:78878000-78879200	Enhancers	GM12878-XiMat	blood
6	chr14:78878000-78880000	Weak transcription	Brain Germinal Matrix	brain
7	chr14:78878400-78878600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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