Variant report

Variant	rs4132712
Chromosome Location	chr5:152165088-152165089
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11167588	0.96[AFR][1000 genomes]
rs11167589	0.91[AFR][1000 genomes]
rs57238654	0.96[AFR][1000 genomes]
rs59533971	0.94[AFR][1000 genomes]
rs60145996	0.94[AFR][1000 genomes]
rs60999611	0.94[AFR][1000 genomes]
rs73272368	0.82[AFR][1000 genomes]
rs73272372	0.96[AFR][1000 genomes]
rs73272373	0.96[AFR][1000 genomes]
rs73272377	0.94[AFR][1000 genomes]
rs73272380	0.96[AFR][1000 genomes]
rs73272382	0.96[AFR][1000 genomes]
rs73272385	0.96[AFR][1000 genomes]
rs73272388	0.96[AFR][1000 genomes]
rs73274581	0.98[AFR][1000 genomes]
rs73274591	0.96[AFR][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	nsv1023676	chr5:151979253-152925064	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv537927	chr5:151979253-152925064	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv883049	chr5:152159184-152399894	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:152165000-152165800	Enhancers	Esophagus	oesophagus

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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