Variant report

Variant	rs74068667
Chromosome Location	chr14:79915122-79915123
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11159410	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56187621	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56376412	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57309646	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57886744	1.00[EUR][1000 genomes]
rs59206596	1.00[EUR][1000 genomes]
rs60526371	1.00[EUR][1000 genomes]
rs60575894	1.00[EUR][1000 genomes]
rs73324284	1.00[EUR][1000 genomes]
rs73326019	1.00[EUR][1000 genomes]
rs73341406	1.00[EUR][1000 genomes]
rs73341410	1.00[EUR][1000 genomes]
rs73341413	1.00[EUR][1000 genomes]
rs73341451	1.00[EUR][1000 genomes]
rs73341454	1.00[EUR][1000 genomes]
rs74068623	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74068628	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs74068669	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74068675	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74068676	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74068677	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74068679	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74068693	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8014580	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931412	chr14:79420297-79928269	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv902110	chr14:79624492-79998294	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv530072	chr14:79769657-79928269	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1045241	chr14:79885361-80734201	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1039622	chr14:79908702-80266601	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79906600-79927000	Weak transcription	Aorta	Aorta
2	chr14:79914200-79915800	Enhancers	Fetal Lung	lung
3	chr14:79915000-79915200	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
4	chr14:79915000-79915400	Enhancers	Stomach Smooth Muscle	stomach
5	chr14:79915000-79916000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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