Variant report

Variant	rs4726220
Chromosome Location	chr7:152586523-152586524
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10225841	0.88[ASN][1000 genomes]
rs10231499	1.00[ASN][1000 genomes]
rs10247318	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10248126	1.00[ASN][1000 genomes]
rs10252415	0.89[ASN][1000 genomes]
rs10256342	0.89[ASN][1000 genomes]
rs10257281	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10261713	1.00[ASN][1000 genomes]
rs12534990	1.00[ASN][1000 genomes]
rs1976876	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36009810	0.98[ASN][1000 genomes]
rs3929596	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4236441	0.94[ASN][1000 genomes]
rs4576342	1.00[ASN][1000 genomes]
rs5013634	1.00[ASN][1000 genomes]
rs5013635	1.00[ASN][1000 genomes]
rs5013637	0.98[ASN][1000 genomes]
rs5013639	0.98[ASN][1000 genomes]
rs55658987	1.00[ASN][1000 genomes]
rs56296501	0.89[ASN][1000 genomes]
rs56729346	1.00[ASN][1000 genomes]
rs57747418	1.00[ASN][1000 genomes]
rs58588589	1.00[ASN][1000 genomes]
rs59178052	1.00[ASN][1000 genomes]
rs59653945	0.94[ASN][1000 genomes]
rs61106470	0.98[ASN][1000 genomes]
rs61701723	1.00[ASN][1000 genomes]
rs61702476	1.00[ASN][1000 genomes]
rs62495011	0.89[ASN][1000 genomes]
rs62495012	0.89[ASN][1000 genomes]
rs6943923	0.94[ASN][1000 genomes]
rs6949453	1.00[ASN][1000 genomes]
rs6969450	1.00[ASN][1000 genomes]
rs6974930	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6977071	1.00[ASN][1000 genomes]
rs6977246	1.00[ASN][1000 genomes]
rs6977266	1.00[ASN][1000 genomes]
rs6977433	1.00[ASN][1000 genomes]
rs73477109	1.00[ASN][1000 genomes]
rs73477118	1.00[ASN][1000 genomes]
rs73493127	0.85[ASN][1000 genomes]
rs73728877	1.00[ASN][1000 genomes]
rs73728880	1.00[ASN][1000 genomes]
rs7795581	0.89[ASN][1000 genomes]
rs7799142	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7799736	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7801501	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033496	chr7:152125903-152615617	Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv539208	chr7:152125903-152615617	Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv1027100	chr7:152294734-152935140	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv831193	chr7:152353544-152592678	Strong transcription Active TSS Genic enhancers Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	nsv532221	chr7:152371297-152884547	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
6	nsv868873	chr7:152371297-152900113	Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
7	nsv532222	chr7:152504090-153450290	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	nsv889506	chr7:152521953-152631037	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1019335	chr7:152546243-152676615	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv539209	chr7:152546243-152676615	Weak transcription Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv508491	chr7:152558615-152588232	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv6008	chr7:152563270-152597257	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	nsv1034937	chr7:152566162-152854895	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	esv3493688	chr7:152574705-152651559	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	esv3493689	chr7:152574764-152651511	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:152578000-152591200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:152581800-152588400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:152581800-152590000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:152583400-152591200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:152585000-152588400	Weak transcription	Gastric	stomach
6	chr7:152586400-152611400	Weak transcription	Right Atrium	heart

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