Variant report

Variant	rs4883744
Chromosome Location	chr13:65669094-65669095
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1340812	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1890283	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4144449	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4453355	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61953883	0.83[EUR][1000 genomes]
rs7318981	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7319969	0.83[EUR][1000 genomes]
rs7324694	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7329489	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7984878	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7985378	0.80[ASN][1000 genomes]
rs9317462	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs9317463	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9528876	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9528889	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9540269	0.83[EUR][1000 genomes]
rs9540270	0.83[EUR][1000 genomes]
rs9540271	0.83[EUR][1000 genomes]
rs9540298	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9540319	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9540330	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9598861	0.82[EUR][1000 genomes]
rs9598879	0.83[EUR][1000 genomes]
rs9598880	0.83[EUR][1000 genomes]
rs9598892	1.00[CEU][hapmap]
rs9598940	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9598945	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045954	chr13:65495013-65842827	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1046706	chr13:65495013-66210226	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv541809	chr13:65495013-66210226	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv900373	chr13:65495897-65775294	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv915632	chr13:65531495-65834877	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv1037329	chr13:65583733-65673656	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
7	esv2761796	chr13:65617000-65688686	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
8	nsv900377	chr13:65620889-65746182	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65664600-65669400	Weak transcription	Fetal Lung	lung

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