Variant report

Variant	rs11013133
Chromosome Location	chr10:18530538-18530539
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18515800-18532000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:18523000-18549400	Weak transcription	Pancreas	Pancrea
3	chr10:18523200-18536000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr10:18526000-18532200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr10:18526200-18536000	Weak transcription	Right Atrium	heart
6	chr10:18527000-18548800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr10:18530000-18532200	Weak transcription	Fetal Heart	heart
8	chr10:18530000-18545200	Weak transcription	Fetal Lung	lung
9	chr10:18530200-18532400	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr10:18530200-18535800	Weak transcription	Left Ventricle	heart
11	chr10:18530200-18543600	Weak transcription	Ovary	ovary
12	chr10:18530400-18532400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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