Variant report

Variant	rs1373674
Chromosome Location	chr4:85352958-85352959
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10005121	0.86[AMR][1000 genomes]
rs10017032	0.91[AMR][1000 genomes]
rs1003159	0.94[AMR][1000 genomes]
rs1003160	0.94[AMR][1000 genomes]
rs1444962	0.94[AMR][1000 genomes]
rs1992653	0.94[AMR][1000 genomes]
rs28513631	0.94[AMR][1000 genomes]
rs28736410	0.94[AMR][1000 genomes]
rs4261980	0.94[AMR][1000 genomes]
rs72955261	0.94[AMR][1000 genomes]
rs72955263	0.94[AMR][1000 genomes]
rs7686486	0.94[AMR][1000 genomes]
rs7692183	0.94[AMR][1000 genomes]
rs7692768	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829997	chr4:85244076-85409405	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv829998	chr4:85299693-85473450	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr4:85352200-85353600	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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