Variant report

Variant	rs73229981
Chromosome Location	chr13:76455511-76455512
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs13378536	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41287014	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41307595	0.90[EUR][1000 genomes]
rs58829651	0.87[EUR][1000 genomes]
rs66538840	0.87[EUR][1000 genomes]
rs68188615	0.83[EUR][1000 genomes]
rs7322777	0.86[EUR][1000 genomes]
rs73227983	0.93[AMR][1000 genomes]
rs73227994	0.86[EUR][1000 genomes]
rs73227996	0.86[EUR][1000 genomes]
rs73229911	0.95[EUR][1000 genomes]
rs73230001	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8001457	0.87[EUR][1000 genomes]
rs9318382	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9318383	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9573666	0.90[EUR][1000 genomes]
rs9573669	0.82[EUR][1000 genomes]
rs9573670	0.95[EUR][1000 genomes]
rs9593139	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9600589	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9600591	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9600592	0.82[AMR][1000 genomes]
rs9600594	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832646	chr13:76300428-76483102	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv2758333	chr13:76321610-76542003	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	esv2759950	chr13:76321610-76542003	Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv832649	chr13:76424872-76657891	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76440000-76469200	Weak transcription	HSMM	muscle
2	chr13:76451800-76463600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr13:76454800-76455600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr13:76454800-76455600	Enhancers	Fetal Stomach	stomach
5	chr13:76455000-76455600	Enhancers	Fetal Kidney	kidney
6	chr13:76455000-76455600	Enhancers	GM12878-XiMat	blood
7	chr13:76455200-76456000	Enhancers	Liver	Liver

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