Variant report

Variant	rs58342688
Chromosome Location	chr4:120654554-120654555
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10016938	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11722660	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11726524	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11730012	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11731926	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11732719	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17005450	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17005667	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17295253	1.00[ASN][1000 genomes]
rs17296412	1.00[ASN][1000 genomes]
rs35428685	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3857096	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55685100	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55717715	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55788903	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55929181	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56291824	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56336246	0.91[ASN][1000 genomes]
rs56337310	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57160305	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57678859	0.96[EUR][1000 genomes]
rs59063054	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60849110	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61595361	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61707138	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs722808	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72906506	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72906508	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72906511	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72906573	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73842698	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73842716	1.00[ASN][1000 genomes]
rs9968281	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv532739	chr4:120392824-121098103	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1010753	chr4:120429028-120684310	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv537233	chr4:120429028-120684310	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1006572	chr4:120432494-120694243	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1802546	chr4:120558608-120675026	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1010638	chr4:120586178-120671835	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1009771	chr4:120590902-120665812	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv1803992	chr4:120649398-120665812	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120649600-120658200	Enhancers	NHLF	lung
2	chr4:120650200-120658000	Enhancers	HSMMtube	muscle
3	chr4:120650200-120658400	Enhancers	NHDF-Ad	bronchial
4	chr4:120650400-120657200	Weak transcription	Psoas Muscle	Psoas
5	chr4:120651200-120656000	Weak transcription	Stomach Smooth Muscle	stomach
6	chr4:120651600-120656000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:120651600-120658000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:120651800-120656000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:120651800-120656000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:120652000-120658600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr4:120652200-120656200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr4:120652200-120656200	Weak transcription	A549	lung
13	chr4:120652200-120658200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr4:120652400-120655800	Weak transcription	HMEC	breast
15	chr4:120652600-120655800	Weak transcription	Colon Smooth Muscle	Colon
16	chr4:120652800-120656000	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr4:120653000-120654600	Weak transcription	NH-A	brain
18	chr4:120653000-120654800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:120653000-120656000	Weak transcription	Hela-S3	cervix
20	chr4:120653200-120654600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr4:120653200-120655200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:120653200-120655800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:120653200-120657200	Weak transcription	Aorta	Aorta
24	chr4:120653400-120654800	Weak transcription	HSMM	muscle
25	chr4:120653400-120655800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr4:120653400-120656000	Weak transcription	Fetal Stomach	stomach
27	chr4:120653400-120656000	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr4:120653400-120656200	Weak transcription	Fetal Kidney	kidney
29	chr4:120653600-120655400	Weak transcription	Fetal Lung	lung
30	chr4:120653600-120655800	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr4:120653600-120656000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:120653600-120656000	Weak transcription	Stomach Mucosa	stomach
33	chr4:120654200-120656000	Weak transcription	Fetal Heart	heart
34	chr4:120654400-120655600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr4:120654400-120658800	Enhancers	Osteobl	bone

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