Variant report

Variant	rs9983032
Chromosome Location	chr21:16515014-16515015
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16511200-16516200	Weak transcription	Adipose Nuclei	Adipose
2	chr21:16512800-16515200	Enhancers	HepG2	liver
3	chr21:16513000-16521600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr21:16514000-16516600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr21:16514200-16515200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr21:16514200-16515400	Weak transcription	Stomach Mucosa	stomach
7	chr21:16514400-16515600	Enhancers	Duodenum Mucosa	Duodenum
8	chr21:16514600-16516000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr21:16514600-16516400	Weak transcription	Pancreas	Pancrea
10	chr21:16514600-16519600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr21:16514600-16529600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr21:16515000-16516000	Weak transcription	Liver	Liver
13	chr21:16515000-16516600	Weak transcription	Small Intestine	intestine

Quick Search:

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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