Variant report

Variant	rs187631468
Chromosome Location	chr3:134432027-134432028
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv528307	chr3:134431174-134433766	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134419800-134432200	Weak transcription	Esophagus	oesophagus
2	chr3:134427800-134433000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr3:134430600-134432200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr3:134431600-134432200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr3:134431600-134432400	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr3:134431600-134432600	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr3:134431600-134433000	Enhancers	Psoas Muscle	Psoas
8	chr3:134432000-134432400	Weak transcription	Osteobl	bone
9	chr3:134432000-134436800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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