Variant report

Variant	rs59288814
Chromosome Location	chr10:25317315-25317316
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25307000-25325400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr10:25314400-25317600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr10:25315400-25317600	Weak transcription	Liver	Liver
4	chr10:25315800-25317400	Weak transcription	NHDF-Ad	bronchial
5	chr10:25316000-25317600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr10:25317000-25317800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr10:25317200-25317800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr10:25317200-25318000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr10:25317200-25318200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr10:25317200-25318200	Enhancers	Osteobl	bone

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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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