Variant report

Variant	rs2695106
Chromosome Location	chr2:178808225-178808226
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1370657	0.95[AFR][1000 genomes]
rs1438052	1.00[AFR][1000 genomes]
rs1898588	0.95[AFR][1000 genomes]
rs2573086	0.89[AFR][1000 genomes]
rs2695095	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2695096	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2695114	0.88[AFR][1000 genomes]
rs2695720	1.00[AFR][1000 genomes]
rs2695721	1.00[AFR][1000 genomes]
rs2695727	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2695759	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56189218	0.95[AFR][1000 genomes]
rs56230218	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56300810	0.88[AFR][1000 genomes]
rs6433700	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6712039	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6752913	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73972662	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73972663	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73972665	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73972667	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73972668	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73972669	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9283485	0.95[AFR][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	nsv533377	chr2:178718801-178963463	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1007579	chr2:178729330-178890946	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv875451	chr2:178748294-178953409	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv998304	chr2:178756380-178924378	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv536056	chr2:178756380-178924378	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv3055	chr2:178800438-178819638	Enhancers Weak transcription	Chromatin interactive region lncRNA	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	chr2:178808200-178808600	Weak transcription	Liver	Liver

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

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