Variant report

Variant	rs59026072
Chromosome Location	chr5:106489820-106489821
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs55714506	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56413244	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58610160	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59563991	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6596728	0.82[AFR][1000 genomes]
rs73777962	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73777965	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73777968	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73777972	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73777977	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73777981	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73777983	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73777987	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73780261	1.00[AMR][1000 genomes]
rs7703722	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7704920	0.86[AFR][1000 genomes];1.00[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	nsv1030118	chr5:106006097-106847949	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv823170	chr5:106326293-106673695	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv599332	chr5:106403516-106502006	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2752056	chr5:106422649-106563101	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1034276	chr5:106461538-106944163	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv537851	chr5:106461538-106944163	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106489200-106490800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:106489400-106491600	Enhancers	Fetal Brain Male	brain

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

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