Variant report

Variant	rs59350680
Chromosome Location	chr8:125033402-125033403
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124971800-125052000	Weak transcription	Gastric	stomach
2	chr8:124990400-125037400	Weak transcription	Fetal Stomach	stomach
3	chr8:125023000-125037000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:125026600-125033800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr8:125031000-125033600	Weak transcription	Left Ventricle	heart
6	chr8:125031000-125048600	Weak transcription	Stomach Mucosa	stomach
7	chr8:125032600-125036000	Enhancers	Primary B cells from peripheral blood	blood
8	chr8:125033000-125033600	Enhancers	GM12878-XiMat	blood
9	chr8:125033200-125034000	Enhancers	Primary B cells from cord blood	blood
10	chr8:125033400-125034600	Enhancers	Fetal Thymus	thymus

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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