Variant report

Variant	rs9282776
Chromosome Location	chr11:33906478-33906479
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33896800-33912200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr11:33902400-33915200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr11:33903800-33910200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr11:33903800-33910600	Enhancers	Primary hematopoietic stem cells	blood
5	chr11:33904000-33906600	Enhancers	K562	blood
6	chr11:33904000-33910800	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr11:33904000-33912000	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr11:33905000-33907200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:33905600-33906600	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr11:33905800-33907000	Enhancers	Spleen	Spleen
11	chr11:33906000-33907400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr11:33906400-33907400	Enhancers	Placenta	Placenta

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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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