Variant report

Variant	rs1602155
Chromosome Location	chr5:57288247-57288248
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10037252	0.96[EUR][1000 genomes]
rs10053148	0.96[EUR][1000 genomes]
rs10054634	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10068767	0.94[EUR][1000 genomes]
rs10080109	0.96[EUR][1000 genomes]
rs1027163	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1037559	0.96[EUR][1000 genomes]
rs10940586	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11743935	0.96[EUR][1000 genomes]
rs1304354	0.96[EUR][1000 genomes]
rs13173455	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs13186838	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs1349955	0.95[EUR][1000 genomes]
rs1349956	1.00[CEU][hapmap];0.92[CHB][hapmap];0.86[JPT][hapmap];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1378246	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1378247	0.96[EUR][1000 genomes]
rs1387634	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1454907	0.95[ASN][1000 genomes]
rs1454916	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1454919	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs1454922	0.96[EUR][1000 genomes]
rs1454923	0.94[EUR][1000 genomes]
rs1489785	0.96[EUR][1000 genomes]
rs1489787	0.96[EUR][1000 genomes]
rs1489788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1489789	0.96[EUR][1000 genomes]
rs1489796	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs1546035	0.96[EUR][1000 genomes]
rs1565339	0.96[EUR][1000 genomes]
rs1809660	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1826098	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1826099	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1840394	0.96[EUR][1000 genomes]
rs1844436	0.96[EUR][1000 genomes]
rs1948276	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2015208	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2198636	0.89[EUR][1000 genomes]
rs4429810	0.96[EUR][1000 genomes]
rs4699919	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6450454	0.96[EUR][1000 genomes]
rs6450455	0.96[EUR][1000 genomes]
rs6450456	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6450457	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6864437	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6892626	0.83[EUR][1000 genomes]
rs7710627	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7714449	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7715831	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs7722307	0.96[EUR][1000 genomes]
rs7725138	0.92[EUR][1000 genomes]
rs9292147	0.96[EUR][1000 genomes]
rs9292149	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9292150	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs971399	0.92[EUR][1000 genomes]
rs995442	0.96[EUR][1000 genomes]
rs995443	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525330	chr5:56931673-57320343	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv1792273	chr5:57214817-57320343	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv10700	chr5:57277483-57313710	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1817904	chr5:57277522-57359476	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1829717	chr5:57277522-57359476	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv1830976	chr5:57277522-57359476	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv1837615	chr5:57277522-57359476	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv1846984	chr5:57277522-57359476	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv1850205	chr5:57277522-57359476	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 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	chr5:57285200-57289200	Weak transcription	Left Ventricle	heart
2	chr5:57285200-57297600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:57286200-57289800	Weak transcription	NHEK	skin
4	chr5:57288200-57288400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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