Variant report

Variant	rs74093589
Chromosome Location	chr13:67635963-67635964
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs55693931	1.00[AMR][1000 genomes]
rs55861079	1.00[AMR][1000 genomes]
rs56143243	1.00[AMR][1000 genomes]
rs56296234	1.00[AMR][1000 genomes]
rs56404521	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57896555	1.00[AMR][1000 genomes]
rs58145156	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58708221	1.00[AMR][1000 genomes]
rs59894116	1.00[AMR][1000 genomes]
rs60474260	1.00[AMR][1000 genomes]
rs61078572	1.00[AMR][1000 genomes]
rs74093405	1.00[AMR][1000 genomes]
rs74093409	1.00[AMR][1000 genomes]
rs74093411	1.00[AMR][1000 genomes]
rs74093488	1.00[AMR][1000 genomes]
rs74093528	1.00[AMR][1000 genomes]
rs74093553	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74093557	1.00[AFR][1000 genomes]
rs74093562	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74093598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74093688	1.00[AMR][1000 genomes]
rs74095121	1.00[AMR][1000 genomes]
rs74095349	1.00[AMR][1000 genomes]
rs74095351	1.00[AMR][1000 genomes]
rs74095354	1.00[AMR][1000 genomes]
rs74095369	1.00[AMR][1000 genomes]
rs74095370	1.00[AMR][1000 genomes]
rs74095372	1.00[AMR][1000 genomes]
rs74095373	1.00[AMR][1000 genomes]
rs74095374	1.00[AMR][1000 genomes]
rs74095375	1.00[AMR][1000 genomes]
rs74095378	1.00[AMR][1000 genomes]
rs74095385	1.00[AMR][1000 genomes]
rs74095390	1.00[AMR][1000 genomes]
rs74095393	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530605	chr13:67126136-67697306	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1035741	chr13:67212973-68077950	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv541817	chr13:67212973-68077950	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv832640	chr13:67460304-67635966	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv428604	chr13:67480426-67645030	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv900414	chr13:67515590-67701341	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1045093	chr13:67517932-67693875	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv541821	chr13:67517932-67693875	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv430581	chr13:67572850-67762288	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv430582	chr13:67589898-67762299	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv1037217	chr13:67589937-67728156	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv1039600	chr13:67593961-67726047	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	nsv541823	chr13:67593961-67726047	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	nsv977372	chr13:67631274-67636478	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67623200-67636000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr13:67626800-67636000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr13:67627800-67636400	Weak transcription	A549	lung
4	chr13:67631400-67636000	Enhancers	Brain Hippocampus Middle	brain
5	chr13:67634000-67636000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr13:67634200-67636000	Enhancers	Brain Angular Gyrus	brain
7	chr13:67634200-67636000	Enhancers	Brain Cingulate Gyrus	brain
8	chr13:67634400-67637200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr13:67634800-67636200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr13:67634800-67636800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr13:67635000-67636000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr13:67635200-67636000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr13:67635400-67636600	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr13:67635600-67645000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr13:67635800-67636000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr13:67635800-67636400	Flanking Active TSS	Brain Anterior Caudate	brain
17	chr13:67635800-67638400	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr13:67635800-67639600	Enhancers	Brain Substantia Nigra	brain

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