Variant report

Variant	rs16874686
Chromosome Location	chr5:5089567-5089568
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11959101	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16874685	0.85[YRI][hapmap];0.93[AMR][1000 genomes]
rs16874715	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57249853	0.82[AMR][1000 genomes]
rs57546252	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59778893	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6555329	0.85[YRI][hapmap];0.93[AMR][1000 genomes]
rs6866197	0.84[YRI][hapmap];0.93[AMR][1000 genomes]
rs6887691	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6898045	0.81[AFR][1000 genomes]
rs73032456	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032459	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032472	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032478	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032481	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73049833	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs73738308	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021653	chr5:4932992-5201887	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv2757980	chr5:4980876-5184615	Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	esv2759318	chr5:4980876-5184615	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv1024784	chr5:4980979-5391231	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv830194	chr5:5002459-5187667	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv10660	chr5:5088517-5095759	Active TSS Enhancers Bivalent/Poised TSS	n/a	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	chr5:5089000-5089600	Bivalent/Poised TSS	HSMMtube	muscle

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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