Variant report

Variant	rs4265980
Chromosome Location	chr2:172470916-172470917
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10432421	0.82[ASN][1000 genomes]
rs10432422	0.82[ASN][1000 genomes]
rs10432470	0.81[ASN][1000 genomes]
rs10432471	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10432472	0.82[ASN][1000 genomes]
rs10432473	0.80[ASN][1000 genomes]
rs11674857	0.82[ASN][1000 genomes]
rs11680728	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11693157	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12472229	0.82[AFR][1000 genomes]
rs12618717	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12622021	0.82[ASN][1000 genomes]
rs12991896	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12997634	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13002792	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13016328	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13025856	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1399960	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1473995	0.82[AFR][1000 genomes]
rs1554157	0.81[ASN][1000 genomes]
rs1554158	0.81[ASN][1000 genomes]
rs1807872	0.82[AFR][1000 genomes]
rs1969271	0.81[ASN][1000 genomes]
rs2037158	0.82[ASN][1000 genomes]
rs2037159	0.82[ASN][1000 genomes]
rs2037161	0.82[ASN][1000 genomes]
rs2037163	0.82[ASN][1000 genomes]
rs2102740	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2138350	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2356796	0.82[ASN][1000 genomes]
rs2356797	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2884028	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34054455	0.88[ASN][1000 genomes]
rs34919335	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35735503	0.88[ASN][1000 genomes]
rs4264541	0.83[ASN][1000 genomes]
rs4265979	0.81[ASN][1000 genomes]
rs4668395	0.82[ASN][1000 genomes]
rs4668396	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57130402	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62181734	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6433301	0.80[ASN][1000 genomes]
rs6433302	0.81[ASN][1000 genomes]
rs6433305	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6704691	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6723896	0.80[ASN][1000 genomes]
rs6743208	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6747069	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6754595	0.81[ASN][1000 genomes]
rs7562302	0.81[ASN][1000 genomes]
rs7571192	0.82[ASN][1000 genomes]
rs7592639	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7606149	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7606189	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7606481	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs908371	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9287946	0.81[ASN][1000 genomes]
rs9678221	0.83[ASN][1000 genomes]
rs997635	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1832950	chr2:172283513-172488111	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv997638	chr2:172442205-172560406	Weak transcription Flanking Active TSS Genic enhancers Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 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	chr2:172469000-172482600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:172470400-172473400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr2:172470600-172471000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr2:172470600-172471200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr2:172470600-172472000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:172470600-172472200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr2:172470800-172471600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr2:172470800-172473600	Enhancers	NHDF-Ad	bronchial
9	chr2:172470800-172474600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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