Variant report

Variant	rs37809
Chromosome Location	chr5:52573292-52573293
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs153129	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs251519	0.88[EUR][1000 genomes]
rs251520	0.88[EUR][1000 genomes]
rs251522	0.88[EUR][1000 genomes]
rs251525	0.88[EUR][1000 genomes]
rs251528	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs252034	0.88[EUR][1000 genomes]
rs252035	0.88[EUR][1000 genomes]
rs252038	0.86[EUR][1000 genomes]
rs252040	0.80[EUR][1000 genomes]
rs252041	0.85[EUR][1000 genomes]
rs252042	0.88[EUR][1000 genomes]
rs252050	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs252051	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs252054	0.84[EUR][1000 genomes]
rs27967	0.89[EUR][1000 genomes]
rs370753	0.88[EUR][1000 genomes]
rs372044	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs37776	0.81[EUR][1000 genomes]
rs37777	0.84[EUR][1000 genomes]
rs37778	0.84[EUR][1000 genomes]
rs37807	0.89[EUR][1000 genomes]
rs38055	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs38056	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs38058	1.00[CEU][hapmap];0.90[MEX][hapmap];0.92[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs384866	0.86[EUR][1000 genomes]
rs40230	0.89[EUR][1000 genomes]
rs40232	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs408393	0.88[EUR][1000 genomes]
rs435548	0.88[EUR][1000 genomes]
rs454737	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs454780	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs565253	0.87[EUR][1000 genomes]
rs574790	0.84[EUR][1000 genomes]
rs584593	0.84[EUR][1000 genomes]
rs626726	0.86[EUR][1000 genomes]
rs629725	0.86[EUR][1000 genomes]
rs664240	0.81[EUR][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	nsv949005	chr5:52188028-52808229	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2752745	chr5:52422063-53343529	Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv830297	chr5:52492494-52707758	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3382349	chr5:52571752-52575051	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52563800-52575200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:52571600-52574000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr5:52572400-52573400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:52572400-52573400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:52572400-52573400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr5:52572400-52573400	Enhancers	HSMM	muscle
7	chr5:52572800-52573600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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