Variant report

Variant	rs7639970
Chromosome Location	chr3:19336826-19336827
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11914667	1.00[EUR][1000 genomes]
rs11915915	1.00[EUR][1000 genomes]
rs11916028	1.00[EUR][1000 genomes]
rs11917497	1.00[EUR][1000 genomes]
rs11918308	1.00[EUR][1000 genomes]
rs11926703	1.00[EUR][1000 genomes]
rs11927110	1.00[EUR][1000 genomes]
rs17005761	1.00[EUR][1000 genomes]
rs34069567	1.00[EUR][1000 genomes]
rs34892402	1.00[EUR][1000 genomes]
rs56969170	1.00[EUR][1000 genomes]
rs57356545	1.00[EUR][1000 genomes]
rs57555741	1.00[EUR][1000 genomes]
rs58683436	1.00[EUR][1000 genomes]
rs59043110	1.00[EUR][1000 genomes]
rs59575962	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60737666	1.00[EUR][1000 genomes]
rs6783211	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6797189	1.00[EUR][1000 genomes]
rs7427695	1.00[EUR][1000 genomes]
rs7624713	1.00[EUR][1000 genomes]
rs7626630	1.00[EUR][1000 genomes]
rs7632339	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7634126	1.00[EUR][1000 genomes]
rs7636919	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7639587	1.00[EUR][1000 genomes]
rs7645122	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7647965	0.92[ASN][1000 genomes]
rs7652572	1.00[EUR][1000 genomes]
rs9817972	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517847	chr3:18845347-19483695	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1010123	chr3:18990307-19989504	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1004602	chr3:19031671-19930052	Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv536511	chr3:19031671-19930052	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv948636	chr3:19335802-19856585	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:19329600-19351400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:19335600-19337200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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