Variant report

Variant	rs16919333
Chromosome Location	chr9:103452327-103452328
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:103450000-103472400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:103450400-103452800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr9:103451200-103452800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:103451200-103453200	Enhancers	Dnd41	blood
5	chr9:103451400-103452800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr9:103451600-103453000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr9:103451800-103452600	Enhancers	Primary T cells from cord blood	blood
8	chr9:103451800-103452800	Enhancers	GM12878-XiMat	blood
9	chr9:103452200-103452800	Enhancers	Thymus	Thymus

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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