Variant report

Variant	rs58213740
Chromosome Location	chr3:179687002-179687003
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11929056	1.00[AMR][1000 genomes]
rs28623139	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829807	chr3:179527567-179745153	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv829808	chr3:179574614-179754321	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv534210	chr3:179666123-179899347	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1000756	chr3:179672703-179827373	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179675800-179688000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr3:179679800-179688000	Weak transcription	Fetal Thymus	thymus
3	chr3:179682200-179688000	Weak transcription	Thymus	Thymus
4	chr3:179684800-179688200	Enhancers	Muscle Satellite Cultured Cells	--
5	chr3:179685400-179687400	Weak transcription	Brain Anterior Caudate	brain
6	chr3:179685800-179687200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr3:179685800-179687800	Weak transcription	HMEC	breast
8	chr3:179686000-179691400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr3:179686200-179687200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr3:179686200-179687200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr3:179686400-179689400	Transcr. at gene 5' and 3'	Dnd41	blood
12	chr3:179686400-179691800	Weak transcription	Osteobl	bone
13	chr3:179686600-179688800	Enhancers	Fetal Brain Male	brain
14	chr3:179686800-179687600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:179686800-179688000	Active TSS	Brain Angular Gyrus	brain
16	chr3:179686800-179688000	Active TSS	Brain Hippocampus Middle	brain
17	chr3:179686800-179692000	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr3:179686800-179692200	Active TSS	Brain Substantia Nigra	brain
19	chr3:179687000-179689400	Active TSS	Brain Cingulate Gyrus	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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