Variant report

Variant	rs28469511
Chromosome Location	chr5:36406001-36406002
allele	A/G
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	chr5:36403400-36406400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr5:36404800-36407000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr5:36405000-36406200	Weak transcription	HSMM	muscle
4	chr5:36405000-36407400	Weak transcription	NH-A	brain
5	chr5:36405200-36406800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr5:36405200-36407400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr5:36405200-36407400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr5:36405200-36407400	Weak transcription	Osteobl	bone
9	chr5:36405800-36408400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr5:36406000-36406200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr5:36406000-36407000	Weak transcription	NHDF-Ad	bronchial
12	chr5:36406000-36407200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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