Variant report

Variant	rs4499117
Chromosome Location	chr13:39516858-39516859
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:19)

rs_ID	r²[population]
rs10870726	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs36098057	0.80[ASN][1000 genomes]
rs3935275	0.83[ASN][1000 genomes]
rs3935279	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4492928	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4608213	0.88[EUR][1000 genomes]
rs4943618	0.83[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs7321316	0.94[EUR][1000 genomes]
rs7986935	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs9315635	0.99[ASN][1000 genomes]
rs9532302	0.80[ASN][1000 genomes]
rs9548541	0.80[ASN][1000 genomes]
rs9548543	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9566378	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9576641	0.80[ASN][1000 genomes]
rs9576642	0.80[ASN][1000 genomes]
rs9576653	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs9576654	0.82[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs9576655	0.82[AFR][1000 genomes];0.92[EUR][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	esv2754118	chr13:39347702-40222644	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1053818	chr13:39512274-39533011	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 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	chr13:39514800-39524200	Weak transcription	H1 BMP4 Derived Mesendoderm 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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