Variant report

Variant	rs72909753
Chromosome Location	chr4:121916330-121916331
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11725572	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12641791	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12643559	0.86[AFR][1000 genomes]
rs12644855	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12646861	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12647946	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28871055	0.86[AFR][1000 genomes]
rs2892918	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4282205	0.88[AFR][1000 genomes]
rs4315815	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4364285	0.86[AFR][1000 genomes]
rs4479732	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56691078	0.88[AFR][1000 genomes]
rs56997621	0.88[AFR][1000 genomes]
rs57429779	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58275100	0.86[AFR][1000 genomes]
rs58383744	0.86[AFR][1000 genomes]
rs59058031	0.88[AFR][1000 genomes]
rs59370413	0.86[AFR][1000 genomes]
rs59750154	0.86[AFR][1000 genomes]
rs60241032	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61592820	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6855125	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72909750	0.85[AFR][1000 genomes]
rs72909791	0.86[AFR][1000 genomes]
rs72909794	0.86[AFR][1000 genomes]
rs72909796	0.82[AFR][1000 genomes]
rs72909798	0.86[AFR][1000 genomes]
rs72909799	0.86[AFR][1000 genomes]
rs72909801	0.86[AFR][1000 genomes]
rs72911603	0.82[AFR][1000 genomes]
rs72911604	0.86[AFR][1000 genomes]
rs72911617	0.86[AFR][1000 genomes]
rs72911625	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72911639	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72911640	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72911643	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72911644	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7698970	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7699505	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9715880	0.88[AFR][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:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121915200-121916400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr4:121915200-121916400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr4:121915200-121916800	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr4:121915400-121917000	Enhancers	Primary T cells from cord blood	blood
5	chr4:121915600-121917000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr4:121915600-121917000	Enhancers	Fetal Lung	lung
7	chr4:121916000-121916800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:121916200-121930800	Weak transcription	H1 Cell Line	embryonic stem cell

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