Variant report

Variant	rs4884722
Chromosome Location	chr13:54429821-54429822
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1379827	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1379831	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1379832	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1379833	0.98[EUR][1000 genomes]
rs1458268	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1545659	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1971924	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1977889	0.98[EUR][1000 genomes]
rs1977890	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs4088520	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6561746	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7334923	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7983436	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7986080	0.90[YRI][hapmap]
rs7995039	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9316660	0.83[EUR][1000 genomes]
rs9536557	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9563174	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9563182	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9563183	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9568906	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9568907	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9568917	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9568919	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9568920	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9568923	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9568924	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9568935	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9568943	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9568948	0.99[EUR][1000 genomes]
rs9591536	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9596858	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9596862	1.00[EUR][1000 genomes];1.00[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	nsv1044137	chr13:54124103-54521120	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv541777	chr13:54124103-54521120	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv427931	chr13:54352943-54543848	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv519254	chr13:54414564-54442809	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv900093	chr13:54414564-54594292	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	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	chr13:54429600-54430200	Active TSS	Esophagus	oesophagus

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