Variant report

Variant	rs4590763
Chromosome Location	chr10:22794748-22794749
allele	A/C
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	chr10:22765800-22806600	Weak transcription	Right Atrium	heart
2	chr10:22790600-22794800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:22790800-22794800	Weak transcription	Primary T cells from cord blood	blood
4	chr10:22791600-22795200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:22793000-22797000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr10:22794000-22796800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr10:22794200-22794800	Bivalent Enhancer	Fetal Lung	lung
8	chr10:22794400-22796200	Enhancers	Primary B cells from peripheral blood	blood
9	chr10:22794600-22795600	Enhancers	Duodenum Mucosa	Duodenum
10	chr10:22794600-22795800	Enhancers	Placenta	Placenta
11	chr10:22794600-22796200	Enhancers	Primary B cells from cord blood	blood
12	chr10:22794600-22796200	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr10:22794600-22796600	Enhancers	Primary T cells fromperipheralblood	blood

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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