Variant report

Variant	rs11059272
Chromosome Location	chr12:123143832-123143833
allele	A/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	chr12:123128200-123147600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:123135800-123152800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr12:123136600-123154200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr12:123140800-123153800	Weak transcription	A549	lung
5	chr12:123141600-123144200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr12:123143800-123144000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:123143800-123144600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr12:123143800-123144600	Enhancers	Primary hematopoietic stem cells	blood
9	chr12:123143800-123144600	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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