Variant report

Variant	rs73324756
Chromosome Location	chr14:79590741-79590742
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs17108386	1.00[AMR][1000 genomes]
rs17108499	1.00[AMR][1000 genomes]
rs17108613	1.00[AMR][1000 genomes]
rs17108638	1.00[AMR][1000 genomes]
rs17108649	1.00[AMR][1000 genomes]
rs1968436	1.00[AMR][1000 genomes]
rs56693583	1.00[AMR][1000 genomes]
rs57057681	1.00[AMR][1000 genomes]
rs57338265	1.00[AMR][1000 genomes]
rs59655196	1.00[AMR][1000 genomes]
rs60009119	1.00[AMR][1000 genomes]
rs61291300	1.00[AMR][1000 genomes]
rs61994014	1.00[AMR][1000 genomes]
rs61995262	1.00[AMR][1000 genomes]
rs61995263	1.00[AMR][1000 genomes]
rs7158612	1.00[AMR][1000 genomes]
rs73317254	1.00[AMR][1000 genomes]
rs73317257	1.00[AMR][1000 genomes]
rs73317263	1.00[AMR][1000 genomes]
rs73317277	1.00[AMR][1000 genomes]
rs73320804	1.00[AMR][1000 genomes]
rs73320805	1.00[AMR][1000 genomes]
rs73320808	1.00[AMR][1000 genomes]
rs73320821	1.00[AMR][1000 genomes]
rs73322875	1.00[AMR][1000 genomes]
rs73322878	1.00[AMR][1000 genomes]
rs73322879	1.00[AMR][1000 genomes]
rs73322888	1.00[AMR][1000 genomes]
rs73323375	1.00[AMR][1000 genomes]
rs73324721	1.00[AMR][1000 genomes]
rs73324743	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73324745	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73324773	1.00[AMR][1000 genomes]
rs73325332	1.00[AMR][1000 genomes]
rs73325337	1.00[AMR][1000 genomes]
rs73325339	1.00[AMR][1000 genomes]
rs73332953	1.00[AMR][1000 genomes]
rs73332961	1.00[AMR][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	nsv1041991	chr14:79394408-79644886	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv931412	chr14:79420297-79928269	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv948724	chr14:79484233-79614043	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2761846	chr14:79522198-79629157	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1040837	chr14:79583862-79711565	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79590600-79590800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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