Variant report

Variant	rs2836577
Chromosome Location	chr21:39998938-39998939
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:39995200-39999200	Weak transcription	Gastric	stomach
2	chr21:39995200-40002400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr21:39996600-40000600	Weak transcription	Aorta	Aorta
4	chr21:39996600-40001800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr21:39997600-39999200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr21:39997600-40000000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr21:39997800-39999400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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