Variant report

Variant	rs73440730
Chromosome Location	chr21:40089069-40089070
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40084600-40089600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr21:40086800-40089200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr21:40088400-40090400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr21:40088600-40089600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr21:40088600-40097000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr21:40088800-40092200	Weak transcription	Dnd41	blood
7	chr21:40089000-40089200	Bivalent Enhancer	HSMMtube	muscle
8	chr21:40089000-40097200	Weak transcription	Aorta	Aorta

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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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