Variant report

Variant	rs73114836
Chromosome Location	chr5:74494611-74494612
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11952940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11955901	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11956613	0.92[EUR][1000 genomes]
rs11959556	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34711940	0.83[AMR][1000 genomes]
rs57091259	1.00[EUR][1000 genomes]
rs57128332	1.00[EUR][1000 genomes]
rs57155346	0.92[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs57350864	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57923199	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58869372	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59226666	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59388080	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs59641773	1.00[EUR][1000 genomes]
rs59992948	0.92[EUR][1000 genomes]
rs60342717	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60349474	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6870950	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6893867	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6894556	1.00[EUR][1000 genomes]
rs6895538	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6898122	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73114819	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73114824	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73114825	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73114854	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73116837	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73116843	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73116846	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73127360	1.00[EUR][1000 genomes]
rs73127366	1.00[EUR][1000 genomes]
rs73127392	1.00[EUR][1000 genomes]
rs73129052	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73131026	0.92[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs73131031	0.84[EUR][1000 genomes]
rs73131051	0.92[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs73131069	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7717760	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7720035	1.00[EUR][1000 genomes]
rs7722905	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	nsv1016610	chr5:74403611-74627654	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv2758000	chr5:74433760-74611714	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2759350	chr5:74433760-74611714	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv882190	chr5:74463185-74554826	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv882191	chr5:74478078-74554826	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74479800-74497000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:74493800-74495000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr5:74494000-74495000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:74494000-74496200	Enhancers	Duodenum Mucosa	Duodenum
5	chr5:74494200-74496200	Enhancers	Fetal Intestine Small	intestine
6	chr5:74494600-74495000	Enhancers	Gastric	stomach
7	chr5:74494600-74495000	Enhancers	Small Intestine	intestine
8	chr5:74494600-74495200	Enhancers	Fetal Intestine Large	intestine
9	chr5:74494600-74495200	Enhancers	Stomach Mucosa	stomach

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