Variant report

Variant	rs73850652
Chromosome Location	chr3:79921091-79921092
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs56364800	0.95[AFR][1000 genomes]
rs58417335	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58872712	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59086056	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59348349	0.84[AFR][1000 genomes]
rs73849750	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73849825	1.00[AMR][1000 genomes]
rs73850426	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73850438	1.00[AMR][1000 genomes]
rs73850439	1.00[AMR][1000 genomes]
rs73850447	0.89[AFR][1000 genomes]
rs73850653	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73853837	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73853841	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73853843	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73853844	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73853845	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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	nsv999796	chr3:79762461-79938163	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv877029	chr3:79824232-79947253	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv834748	chr3:79828668-79985688	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:79917400-79927400	Weak transcription	Aorta	Aorta
2	chr3:79918000-79921200	Enhancers	Fetal Lung	lung
3	chr3:79919600-79922800	Enhancers	HUVEC	blood vessel
4	chr3:79920400-79921200	Enhancers	Ovary	ovary
5	chr3:79920400-79922400	Enhancers	NH-A	brain
6	chr3:79920400-79923000	Enhancers	Hela-S3	cervix
7	chr3:79920400-79925000	Enhancers	Fetal Heart	heart

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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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