Variant report

Variant	rs2909827
Chromosome Location	chr5:116062476-116062477
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs2909818	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2909820	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2909821	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2909824	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2909826	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2933594	0.88[EUR][1000 genomes]
rs2933595	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2933597	0.84[EUR][1000 genomes]
rs2933604	0.80[EUR][1000 genomes]
rs2933624	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2933636	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2964650	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2964685	0.81[EUR][1000 genomes]
rs2964686	0.88[EUR][1000 genomes]
rs2964687	0.88[EUR][1000 genomes]
rs2964688	0.88[EUR][1000 genomes]
rs2964689	0.88[EUR][1000 genomes]
rs2964690	0.88[EUR][1000 genomes]
rs4512158	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7707373	0.89[EUR][1000 genomes]
rs872411	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs878401	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763490	chr5:115918339-116138525	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv830456	chr5:115969066-116170718	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv527974	chr5:115987168-116303678	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv462403	chr5:115994775-116284378	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv599485	chr5:115994775-116284378	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1030056	chr5:116008971-116278725	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1033140	chr5:116035131-116314673	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116061400-116068200	Enhancers	Fetal Heart	heart
2	chr5:116062000-116064400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr5:116062000-116067400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:116062400-116062600	Enhancers	HUES6 Cell Line	embryonic stem cell

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