Variant report

Variant	rs4132382
Chromosome Location	chr5:118042467-118042468
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10065855	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10068737	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10070652	0.88[EUR][1000 genomes]
rs10070670	0.88[EUR][1000 genomes]
rs10072500	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10078607	0.87[EUR][1000 genomes]
rs10477578	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10900724	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11241471	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12655864	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1366981	0.91[EUR][1000 genomes]
rs1429705	0.90[EUR][1000 genomes]
rs1429706	0.91[EUR][1000 genomes]
rs1429707	0.91[EUR][1000 genomes]
rs1429708	0.91[EUR][1000 genomes]
rs1429709	0.91[EUR][1000 genomes]
rs2376683	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34424553	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4895158	0.88[EUR][1000 genomes]
rs58276178	0.88[EUR][1000 genomes]
rs734513	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs734514	0.80[AMR][1000 genomes];0.91[EUR][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	nsv599541	chr5:117869174-118049776	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1032241	chr5:117900051-118157400	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv882767	chr5:117931730-118385691	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118040600-118042800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:118041000-118042800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:118041000-118042800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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Input of quick search could be:

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

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