Variant report

Variant	rs4681058
Chromosome Location	chr3:25440041-25440042
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12330681	0.99[ASN][1000 genomes]
rs12490801	0.93[ASN][1000 genomes]
rs13088742	0.94[ASN][1000 genomes]
rs17523903	0.94[ASN][1000 genomes]
rs2116702	0.97[ASN][1000 genomes]
rs36013124	0.90[ASN][1000 genomes]
rs62237590	0.94[ASN][1000 genomes]
rs7634400	0.94[ASN][1000 genomes]
rs7650761	0.94[ASN][1000 genomes]
rs7653107	0.90[ASN][1000 genomes]
rs922941	0.91[ASN][1000 genomes]
rs962926	0.91[ASN][1000 genomes]
rs9834839	0.94[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	nsv949035	chr3:25194301-26084890	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
2	nsv834645	chr3:25363723-25555107	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr3:25437800-25440400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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