Variant report

Variant	rs16865933
Chromosome Location	chr2:178800436-178800437
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10497485	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10497486	1.00[AMR][1000 genomes]
rs1370658	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1527292	1.00[AMR][1000 genomes]
rs16865829	1.00[AMR][1000 genomes]
rs16865833	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865835	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865838	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865839	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865844	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865848	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865850	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865852	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865872	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865887	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865907	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865909	1.00[AMR][1000 genomes]
rs16865912	0.91[AFR][1000 genomes]
rs16865918	0.81[AFR][1000 genomes];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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178800200-178800600	Enhancers	Fetal Brain Male	brain

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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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