Variant report

Variant	rs72895475
Chromosome Location	chr3:80025889-80025890
allele	A/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]
rs17017453	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41501345	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57049976	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72895458	0.82[AFR][1000 genomes]
rs72895470	0.82[AFR][1000 genomes]
rs72895477	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72895478	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72895480	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72895481	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72895486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72895487	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72895490	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72897318	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72897331	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7622614	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7632598	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	nsv1009391	chr3:79604443-80035898	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv428088	chr3:79934080-80112721	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv590740	chr3:79999534-80575042	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv997786	chr3:80008898-80489031	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv536598	chr3:80008898-80489031	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv877030	chr3:80013063-80444843	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 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	chr3:80023600-80026000	Weak transcription	NH-A	brain
2	chr3:80025600-80026800	Enhancers	HUVEC	blood vessel

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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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