Variant report

Variant	rs58784157
Chromosome Location	chr8:59075351-59075352
allele	C/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	chr8:59068400-59085000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:59069600-59075600	Weak transcription	Fetal Stomach	stomach
3	chr8:59069800-59076000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:59074000-59075600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:59074200-59075400	Enhancers	HepG2	liver
6	chr8:59074600-59075600	Enhancers	GM12878-XiMat	blood
7	chr8:59074800-59083200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr8:59075000-59075400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:59075000-59082000	Weak transcription	Fetal Muscle Leg	muscle
10	chr8:59075200-59075600	Enhancers	Primary monocytes fromperipheralblood	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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