Variant report

Variant	rs56967455
Chromosome Location	chr5:93875239-93875240
allele	A/T
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:12)

rs_ID	r²[population]
rs57922034	1.00[AMR][1000 genomes]
rs6881189	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73134676	1.00[AMR][1000 genomes]
rs73145038	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73145048	1.00[AMR][1000 genomes]
rs73145052	0.80[AFR][1000 genomes]
rs73145053	0.80[AFR][1000 genomes]
rs73145055	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73145060	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73145064	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73145066	1.00[AMR][1000 genomes]
rs73145080	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023191	chr5:93351646-93947928	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv537808	chr5:93351646-93947928	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1023421	chr5:93679661-93911066	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	esv2758002	chr5:93765205-94042201	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	esv2759354	chr5:93765205-94042201	Active TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv534495	chr5:93789736-93962131	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv598952	chr5:93823951-93956986	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:93855400-93886400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr5:93856200-93882600	Weak transcription	Ovary	ovary
3	chr5:93867000-93880600	Weak transcription	Spleen	Spleen
4	chr5:93868000-93879800	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr5:93868200-93875800	Weak transcription	Fetal Lung	lung
6	chr5:93868400-93878800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:93868600-93879800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr5:93872800-93881600	Weak transcription	Pancreas	Pancrea
9	chr5:93873600-93878800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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