Variant report

Variant	rs2937532
Chromosome Location	chr5:36402114-36402115
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36391200-36403200	Weak transcription	Placenta	Placenta
2	chr5:36393800-36403600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr5:36394000-36402600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:36394000-36402800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr5:36394800-36402800	Weak transcription	HSMM	muscle
6	chr5:36398400-36402200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr5:36398400-36402600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:36398400-36402800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:36398400-36402800	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr5:36398400-36402800	Weak transcription	Osteobl	bone
11	chr5:36398400-36403600	Weak transcription	Colon Smooth Muscle	Colon
12	chr5:36398400-36403600	Weak transcription	Fetal Lung	lung
13	chr5:36398600-36402200	Weak transcription	NHDF-Ad	bronchial
14	chr5:36400400-36402800	Enhancers	HepG2	liver
15	chr5:36400600-36404000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr5:36400600-36405200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr5:36401200-36402200	Enhancers	Liver	Liver
18	chr5:36401400-36402600	Weak transcription	NHLF	lung
19	chr5:36401800-36402600	Weak transcription	Primary B cells from peripheral blood	blood

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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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