Variant report

Variant	rs16996603
Chromosome Location	chr21:39997541-39997542
allele	A/G
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	chr21:39989200-39997600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr21:39995200-39999200	Weak transcription	Gastric	stomach
3	chr21:39995200-40002400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr21:39996600-40000600	Weak transcription	Aorta	Aorta
5	chr21:39996600-40001800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr21:39997400-39997600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr21:39997400-39997800	Enhancers	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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