Variant report

Variant	rs7669591
Chromosome Location	chr4:98832479-98832480
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10013348	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1084778	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1084779	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11939317	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1215053	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12640735	0.93[ASN][1000 genomes]
rs12640871	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12648529	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs165240	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs165243	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs165248	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs165249	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs165253	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17027012	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17027019	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs184816	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2605542	0.88[ASN][1000 genomes]
rs260891	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs260900	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs260903	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs356548	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs589940	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs595656	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60404606	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6813356	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6814180	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6844839	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6858639	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72686424	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72686434	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72686436	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72686449	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7673305	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs783919	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs783920	0.82[ASN][1000 genomes]
rs783926	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs783927	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs783935	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs783944	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs783946	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs783948	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs783953	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs783954	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs783956	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9684842	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879643	chr4:98317295-99065480	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv868914	chr4:98416047-98969285	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1012612	chr4:98433491-98949873	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1002098	chr4:98501337-99086320	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv537193	chr4:98501337-99086320	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv529623	chr4:98501338-99460166	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
7	nsv1010982	chr4:98529206-98841438	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv537194	chr4:98529206-98841438	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv879648	chr4:98547717-99104879	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv1000011	chr4:98562308-99101692	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv879649	chr4:98652600-98873667	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv932060	chr4:98696832-98902498	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv1000956	chr4:98732458-99178588	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv999087	chr4:98737003-98860303	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv594937	chr4:98748299-98866902	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv530387	chr4:98757752-98922248	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
17	nsv1005567	chr4:98779722-99031934	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
18	nsv995045	chr4:98802844-99022958	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98831400-98832600	Weak transcription	Pancreas	Pancrea
2	chr4:98831600-98839200	Weak transcription	Gastric	stomach
3	chr4:98832200-98832800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:98832200-98832800	Enhancers	Fetal Muscle Trunk	muscle
5	chr4:98832200-98833000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:98832200-98833200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:98832400-98832800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr4:98832400-98832800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:98832400-98832800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:98832400-98833200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast

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