Variant report

Variant	rs62320719
Chromosome Location	chr4:120274210-120274211
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs11722940	0.91[ASN][1000 genomes]
rs11724619	0.91[ASN][1000 genomes]
rs11725433	0.80[ASN][1000 genomes]
rs11727068	0.89[AMR][1000 genomes]
rs11728178	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11729960	0.91[ASN][1000 genomes]
rs11733606	0.80[ASN][1000 genomes]
rs11734808	0.91[ASN][1000 genomes]
rs11735260	0.89[AMR][1000 genomes]
rs11736997	0.91[ASN][1000 genomes]
rs11737068	0.91[ASN][1000 genomes]
rs13104050	0.80[ASN][1000 genomes]
rs13112320	0.91[ASN][1000 genomes]
rs13113462	0.80[ASN][1000 genomes]
rs13113662	0.80[ASN][1000 genomes]
rs13122306	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs13127517	0.81[ASN][1000 genomes]
rs13139711	0.96[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13140255	0.80[ASN][1000 genomes]
rs13144426	0.80[ASN][1000 genomes]
rs1397611	0.91[ASN][1000 genomes]
rs17050312	0.91[ASN][1000 genomes]
rs17334151	0.80[ASN][1000 genomes]
rs17517470	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs17595468	0.91[ASN][1000 genomes]
rs17595769	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs17595790	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2036859	0.91[ASN][1000 genomes]
rs34125807	0.91[ASN][1000 genomes]
rs34156358	0.80[ASN][1000 genomes]
rs34733524	0.91[ASN][1000 genomes]
rs34878806	0.91[ASN][1000 genomes]
rs34951506	0.80[ASN][1000 genomes]
rs35137697	0.80[ASN][1000 genomes]
rs35225855	0.91[ASN][1000 genomes]
rs35612705	0.80[ASN][1000 genomes]
rs35646004	0.80[ASN][1000 genomes]
rs35846514	0.91[ASN][1000 genomes]
rs35917388	0.91[ASN][1000 genomes]
rs3817230	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3817242	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs56818816	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs62320715	0.91[ASN][1000 genomes]
rs62320716	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320717	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320718	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320720	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320721	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320722	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320723	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320724	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320725	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320731	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320732	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320733	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320735	0.96[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62320737	0.91[ASN][1000 genomes]
rs62328380	0.80[ASN][1000 genomes]
rs62328402	0.80[ASN][1000 genomes]
rs62328403	0.80[ASN][1000 genomes]
rs62328404	0.80[ASN][1000 genomes]
rs62328408	0.91[ASN][1000 genomes]
rs62328420	0.91[ASN][1000 genomes]
rs6822097	0.80[ASN][1000 genomes]
rs71627784	0.90[ASN][1000 genomes]
rs72918504	0.96[AMR][1000 genomes];0.91[ASN][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	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1012868	chr4:120014630-120464880	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv537232	chr4:120014630-120464880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv428769	chr4:120205572-120363323	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv879841	chr4:120244085-120388406	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv879842	chr4:120244085-120424087	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv427694	chr4:120250511-120501728	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	esv2538163	chr4:120252854-120388678	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv964091	chr4:120255342-120290951	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding 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	chr4:120266400-120275000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr4:120269200-120277600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr4:120269600-120293000	Weak transcription	Fetal Heart	heart
4	chr4:120273800-120275200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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