Variant report

Variant	rs7006498
Chromosome Location	chr8:125024181-125024182
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 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	chr8:125021400-125024800	Enhancers	K562	blood
4	chr8:125022400-125030600	Weak transcription	Stomach Mucosa	stomach
5	chr8:125023000-125025000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr8:125023000-125037000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:125023800-125025000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:125024000-125024800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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