Variant report

Variant	rs34659347
Chromosome Location	chr4:121923570-121923571
allele	G/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]
rs1020500	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12108250	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12108616	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13108580	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1450467	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1450468	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1817034	1.00[ASN][1000 genomes]
rs34433706	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34498056	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34760476	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35386491	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35402261	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36089502	1.00[ASN][1000 genomes]
rs3956526	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4075801	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4426804	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4435764	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4488957	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59229457	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6814333	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6816015	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6819558	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6825861	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6829576	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6832312	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6841260	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6858077	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71602306	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7675722	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7690755	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][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	nsv998094	chr4:121504565-122374203	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1009395	chr4:121841442-122557363	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv537235	chr4:121841442-122557363	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv3386870	chr4:121867625-122208448	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv879859	chr4:121892490-122438312	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121916200-121930800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr4:121923000-121925200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:121923000-121927000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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