Variant report

Variant	rs62323674
Chromosome Location	chr4:54537769-54537770
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs4864806	0.86[EUR][1000 genomes]
rs55843256	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56314005	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62323675	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62323676	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62323677	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62323679	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62323680	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62323681	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62323682	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62325510	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73250977	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73250980	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829936	chr4:54367783-54556123	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:54536800-54538200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr4:54536800-54539000	Enhancers	Liver	Liver
3	chr4:54537200-54542400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:54537400-54538000	Enhancers	Fetal Heart	heart
5	chr4:54537400-54538000	Weak transcription	Ovary	ovary

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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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