Variant report

Variant	rs72979522
Chromosome Location	chr3:134866845-134866846
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1501219	1.00[ASN][1000 genomes]
rs58368140	1.00[ASN][1000 genomes]
rs72977587	1.00[ASN][1000 genomes]
rs72979526	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1000277	chr3:134546080-134970837	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv877516	chr3:134689420-134918522	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv829731	chr3:134711713-134885064	Strong transcription Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	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	chr3:134823000-134880000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:134859200-134869800	Enhancers	Liver	Liver
3	chr3:134859600-134873600	Weak transcription	Right Ventricle	heart
4	chr3:134860800-134867800	Weak transcription	Psoas Muscle	Psoas
5	chr3:134861000-134878200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:134861400-134867200	Weak transcription	Fetal Brain Male	brain
7	chr3:134861600-134880600	Weak transcription	Fetal Brain Female	brain
8	chr3:134864800-134870200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr3:134865800-134868000	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr3:134866000-134867800	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr3:134866000-134868000	Enhancers	Brain Angular Gyrus	brain
12	chr3:134866200-134867600	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr3:134866400-134868000	Enhancers	Brain Anterior Caudate	brain
14	chr3:134866400-134868000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr3:134866400-134868000	Enhancers	Brain Substantia Nigra	brain
16	chr3:134866400-134868600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr3:134866400-134868600	Enhancers	Brain Hippocampus Middle	brain
18	chr3:134866600-134867000	Weak transcription	Right Atrium	heart
19	chr3:134866600-134869000	Enhancers	Brain Cingulate Gyrus	brain

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Input of quick search could be:

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

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