Variant report

Variant	rs17051345
Chromosome Location	chr4:120576634-120576635
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12108288	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17050700	1.00[ASN][1000 genomes]
rs17051339	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2127822	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2389889	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2389890	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4314268	1.00[ASN][1000 genomes]
rs4833623	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4834795	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57391877	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6823633	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6842758	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6844418	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72924305	0.80[AFR][1000 genomes]
rs73842682	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73842683	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7670921	1.00[CEU][hapmap]
rs7690175	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9997186	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 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

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120568400-120577400	Weak transcription	Psoas Muscle	Psoas
2	chr4:120568600-120582200	Weak transcription	Fetal Brain Male	brain
3	chr4:120573800-120578600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:120574000-120576800	Weak transcription	Aorta	Aorta
5	chr4:120574200-120577600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:120574600-120577400	Weak transcription	NH-A	brain
7	chr4:120574600-120577800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr4:120574600-120578200	Weak transcription	NHDF-Ad	bronchial
9	chr4:120574800-120577600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:120574800-120578000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr4:120575600-120581400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:120575800-120576800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:120576200-120576800	Enhancers	Osteobl	bone
14	chr4:120576200-120579000	Enhancers	HUVEC	blood vessel
15	chr4:120576400-120576800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr4:120576400-120578600	Enhancers	Fetal Lung	lung
17	chr4:120576600-120579000	Enhancers	NHLF	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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