Variant report

Variant	rs373628281
Chromosome Location	chr5:57487603-57487604
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	nsv969959	chr5:57486620-57495174	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57483000-57488400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr5:57484200-57488200	Enhancers	Hela-S3	cervix
3	chr5:57485400-57487800	Weak transcription	Adipose Nuclei	Adipose
4	chr5:57485800-57490400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:57486000-57488200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:57486800-57488000	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr5:57487000-57487800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:57487200-57488200	Enhancers	HMEC	breast
9	chr5:57487400-57488000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr5:57487600-57488200	Enhancers	A549	lung

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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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